INTRODUCTION

Top Abstract Introduction Materials and Methods Results Discussion References

Anaplasma marginale is an important tick-transmitted rickettsial pathogen of cattle that invades and multiplies within erythrocytes, causing severe hemolytic anemia during acute infection. Recovery from acute disease leads to a state of persistent infection and allows subsequent transmission to immunologically naïve cattle. At least six outer membrane proteins (OMP) of A. marginale have been described (32, 34), and major surface protein 2 (MSP-2) is among the most immunodominant surface antigens. A. marginale is a member of the ehrlichial genogroup II, and MSP-2 shares significant structural and sequence homology with OMP homologues of other ehrlichiae. These include members of genogroup II, most notably the agent of human granulocytic ehrlichiosis (HGE), and the genogroup I pathogens Ehrlichia chaffeensis and Cowdria ruminantium (14, 18, 27, 30, 36, 51, 53).

Immunization with native MSP-2 derived from the Florida strain of A. marginale resulted in partial to complete protection in cattle challenged with homologous or heterologous strains (31). Immunization with outer membranes of A. marginale also provided protection to 70% of calves, and protection correlated with titers of antibody against MSP-2 (46). Furthermore, members of our group recently demonstrated complete protection against infection following homologous challenge in calves immunized with purified outer membranes of the Florida strain with saponin as an adjuvant (7). Complete protection was associated with development of immunoglobulin G2 (IgG2) responses directed predominantly against MSP-2 and with the production of gamma interferon (IFN-) by antigen-specific T cells. Several cloned CD4⁺ T-cell lines derived from the protected cattle were MSP-2 specific, but not strain specific, suggesting recognition of MSP-2 T-cell epitopes conserved among strains (9). This conservation is notable given the extensive structural variation encoded by the msp2 gene family, both within and between strains (15, 31, 34, 39). Thus, such conserved T-cell epitopes may be useful components of a subunit or nucleic acid vaccine designed to induce protective immunity against multiple strains of A. marginale.

CD4⁺ T cells are important for immunity against intraerythrocytic pathogens by activating macrophages through the production of IFN- (44) and by promoting enhanced IgG production (6). The importance of IFN- in protection against anaplasmosis has been recently reviewed (34). Briefly, in cattle IFN- enhances IgG2 production (6, 10), and activates macrophages to produce molecules, such as nitric oxide (NO), that are toxic for intraerythrocytic pathogens (references 20 and 44; L. K. M. Shoda, J. Florin-Christenson, M. Florin-Christenson, G. H. Palmer, and W. C. Brown, submitted for publication). In vitro incubation with A. marginale-immune serum neutralized the infectivity of A. marginale for cattle (33), and IgG2 may be involved in neutralization because of its superior ability to promote phagocytosis through opsonization (25). For these reasons, adjuvants that stimulate the production of IFN- during antigen priming and IgG antibodies are predicted to enhance protective immune responses.

IL-12 is a cytokine that when used as an adjuvant with a protein antigen can augment protective immunity against intracellular pathogens by stimulating IFN- production (1, 26). Numerous studies in mice have verified that interleukin-12 (IL-12), produced by dendritic cells and other antigen-presenting cells (APC) during T-cell priming, promotes a biased or enhanced Th1 cytokine response (17, 24, 40, 41, 43, 45, 47). When adsorbed together with a soluble protein in aluminum hydroxide (alum), IL-12 stimulated a polarized type 1 cytokine response but enhanced both type 1 (IgG2 and IgG3) and type 2 (IgG1) antibody responses in mice (19). Adsorption of IL-12 to alum appeared critical for maintaining serum IFN- levels, likely by prolonging the in vivo half-life of IL-12. Recently, it was demonstrated that the recall T-cell response to a protein antigen administered with IL-12 in phosphate buffered saline (PBS) during the primary antigen inoculation featured the type 1 cytokine and antibody responses observed immediately after priming. Interestingly, the memory response to antigen was additionally characterized by the development of type 2 cytokine and antibody responses not observed after priming (3). In vivo experiments performed with IL-12 as an adjuvant for cattle have not been reported. However, IL-12 stimulated enhanced IFN- production by mitogen- or antigen-stimulated bovine peripheral blood mononuclear cells (PBMC) and antigen-stimulated effector CD4⁺ T-cell clones (4). Furthermore, when added during in vitro activation and differentiation of memory T cells cultured with antigen, IL-12 induced production of IFN- that was significantly enhanced compared to that of cells cultured without exogenous IL-12 (49). In the present study, we hypothesized that IL-12 administered as an adjuvant to cattle with MSP-2 by coadsorption to alum would prime for enhanced type 1 recall responses characterized by increased production of IFN- in response to A. marginale stimulation by memory or effector CD4⁺ T cells. We observed that IL-12 stimulated enhanced IFN- and IL-2 secretion and transcript expression by antigen-primed lymph node cells (LNC) as well as enhanced serum IgG1 titers. Transcript levels of IL-4 and IL-10 were also elevated in LNC from IL-12-primed calves. Contrary to what was predicted, IL-12 did not uniformly stimulate IgG2 production, and the upregulation of IgG2 by one calf given IL-12 was not associated with high levels of IFN- production. These data suggest that factors in addition to IFN- may be important for promoting isotype switching to IgG2.

	MATERIALS AND METHODS

Top Abstract Introduction Materials and Methods Results Discussion References

Preparation of A. marginale antigens. A splenectomized Holstein calf was infected with A. marginale (Florida strain) to propagate organisms for preparation of outer membranes and purified MSP-2. Native MSP-2 was gel purified to ensure that all of the potentially expressed MSP-2 copies in the Florida strain were represented in the immunogen. A. marginale organisms were isolated from thawed, infected bovine erythrocytes by sonication and differential ultracentrifugation as previously described (33), suspended in electrophoresis sample buffer, and separated on multiple preparative sodium dodecyl sulfate (SDS)-10% polyacrylamide gels. One gel was transferred and blotted with MSP-2-specific monoclonal antibody (MAb) as described previously (31) to orient the MSP-2 on the preparative gels. The MSP-2 band was excised from multiple gels, and the protein was electroeluted from the gel fragments as described previously (29). Eluted protein was concentrated and dialyzed against PBS (pH 7.2) and repurified a second time on preparative gels. Figure 1 shows the result of a SDS-12% polyacrylamide gel electrophoresis (SDS-12% PAGE) analysis of 3 µg of gel-purified MSP-2 used for inoculation. MSP-2 was verified by immunoblotting to be reactive with the antibodies specific for MSP-2 but unreactive with antibodies to other A. marginale MSP (data not shown).

View larger version (53K): [in this window] [in a new window]   FIG. 1.   SDS-PAGE analysis of gel-purified native MSP-2 from the Florida strain of A. marginale. MSP-2 (3 µg) was visualized on a Coomassie blue-stained 12% acrylamide gel (arrow). Molecular masses are indicated on the right of the gel.

Cattle and immunization with MSP-2. Nine age-matched Holstein steers 4 to 5 months old and weighing approximately 150 to 200 kg at the start of the experiment were verified to be serologically negative for A. marginale by competitive inhibition enzyme-linked immunosorbent assay (ELISA) (21) and were assigned randomly to three groups. All calves received six 2-ml subcutaneous inoculations in the right and left sides of the neck as detailed in Table 1. Calves were administered alum and IL-12 (group I); alum and MSP-2 (group II); or alum, MSP-2, and IL-12 (group III). Human recombinant IL-12 was kindly provided by Genetics Institute, Inc., Cambridge, Mass. The dosage of IL-12 (approximately 50 ng/kg of body weight) used was 10-fold less than that used in human trials where toxicity was observed (22). In initial inoculations, 20 µg of MSP-2 was given, since this amount of antigen induced vigorous responses in other immunization studies (reference 37; W. C. Brown, T. C. McGuire, and G. H. Palmer, unpublished observations). After two injections, the amount of MSP-2 was increased, since weak antibody and proliferation responses were generated. Gel-purified MSP-2 and/or IL-12 was adsorbed in 20 mg of alum (Rehydragel, low viscosity sterile gel; Reheis, Inc., Berkeley Heights, N.J.) in 2 ml of sterile PBS according to the manufacturer's instructions. Serum samples and PBMC were collected before and at 2 weeks following each inoculation and assayed for A. marginale-specific antibody and proliferation, respectively. Once specific lymphocyte proliferation was observed, the animals were given a final antigen inoculation and the antigen-draining (right) and contralateral (left) prescapular lymph nodes (LN) were surgically biopsied to remove approximately one half of the LN. The timing of the sixth inoculation was staggered so that one calf per group was used at each time point (Table 1). LNC suspensions were prepared (38) and either were used immediately for proliferation assays, surface phenotype analysis, and cytokine determination or were cryopreserved in liquid nitrogen in a solution of 10% dimethylsulfoxide in fetal bovine serum.

Analysis of A. marginale-specific IgG1 and IgG2 responses. SDS-PAGE and immunoblotting were performed with MAb specific for bovine IgG, IgG1, and IgG2 to determine the appearance of MSP-2-specific antibody and the subclass of the specific IgG response. The procedures were performed as described recently (7), with the following modifications. A. marginale (Florida strain) homogenate (100 µg of protein) was applied in a single lane to a 7.5 to 17.5% polyacrylamide gradient gel and electrophoresed, and the proteins were transferred to nitrocellulose membranes. The membranes were air-dried and immersed for 2 h in blocking solution consisting of PBS (pH 7.4) supplemented with 0.02% sodium azide, 0.1% Tween 20, and 10% normal horse serum (Vector Laboratories, Inc., Burlingame, Calif.) with gentle agitation. Following extensive washing in PBS-Tween (PBS [pH 7.4]-0.02% sodium azide-0.1% Tween 20), the membranes were placed in a Miniblotter 25 apparatus (Immunetics, Cambridge, Mass.) and 250 µl of bovine sera serially diluted (1:100 to 1:100,000) in blocking solution per well was added according to the manufacturer's protocol. The membranes were incubated for 2 h at room temperature on a rocking platform. Following successive washes in PBS-Tween with 0.1% NP-40 and PBS-Tween alone, the membranes were incubated overnight at 4°C and for an additional 1.5 h at room temperature on a rocker platform with murine anti-bovine IgG, IgG1, or IgG2 MAb (Serotec Ltd., Oxford, United Kingdom) diluted 1:100 in PBS-Tween with 2% horse serum. The membranes were washed extensively, and the reaction mixtures were then labeled for 1 h at room temperature with peroxidase-conjugated affinity-purified donkey anti-mouse IgG (heavy plus light chains; Jackson Immunoresearch Laboratories, West Grove, Pa.) diluted 1:5,000 in TNT buffer containing 1% horse serum. The membranes were washed repeatedly with TNT buffer, and the chemiluminescence was developed with a Renaissance Western blot chemiluminescence reagent (NEN Life Science Products, Boston, Mass.) according to the manufacturer's instructions.

A. marginale-specific T-cell lines. Short-term T-cell lines were established from PBMC of A. marginale MSP-2-immunized calves from 3 to 5 weeks following the fifth immunization or from cryopreserved LNC. Briefly, 4 × 10⁶ PBMC or LNC per well were cultured in 24-well plates (Costar, Cambridge, Mass.) in 1.5 ml of complete RPMI 1640 medium (5) with 3 to 5 µg of A. marginale membrane antigen per ml. After 7 days, cells were subcultured to a density of 5 × 10⁵ cells per well and cultured with antigen and 2 × 10⁶ irradiated (3,000 rads) autologous PBMC as a source of APC. T-cell lines were maintained for up to 5 weeks by weekly stimulation with antigen and APC, and cells were assayed for antigen-dependent proliferation 7 days following the last stimulation.

Lymphocyte proliferation assays. Proliferation assays were carried out in replicate wells of round-bottomed 96-well plates (Costar) for 5 to 6 days when PBMC were used or for 4 days when LNC or short-term T-cell lines were used, essentially as described previously (7, 9). PBMC or LNC (2 × 10⁵) were cultured in triplicate wells with antigen in a total volume of 100 µl of complete medium. T-cell lines were assayed 7 days after the last stimulation with antigen and APC. T-cell lines (3 × 10⁴ cells) were cultured in duplicate wells in a total volume of 100 µl of complete medium containing 2 × 10⁵ APC and antigen. Antigens consisted of 0.2 to 25.0 µg of A. marginale Florida homogenate or membranes per ml, and as a control, membranes prepared from uninfected bovine red blood cells (URBC) (6) were used. Protein concentrations in all antigen preparations were determined by the Bradford assay. To determine proliferation, cells were radiolabeled for the last 18 h of culture with 0.25 µCi of [³H]thymidine (Dupont New England Nuclear, Boston, Mass.), radiolabeled nucleic acids were harvested onto glass filters, and radionucleotide incorporation was measured with a Betaplate 1205 liquid scintillation counter (Wallac, Gaithersburg, Md.). Results presented are the mean number of counts per minute of replicate cultures ± the standard error of the mean (SEM) or the stimulation index (SI), which represents the mean number of counts per minute of replicate cultures of cells plus antigen/the mean number of counts per minute of replicate cultures of cells plus medium or URBC. An SI of 2.0 was considered statistically significant.

Cell-surface phenotypic analysis. Differentiation markers on LNC and T-cell lines were analyzed by indirect immunofluorescence and flow cytometry as previously described (8). The MAbs used were specific for bovine CD2 (MAb MUC2A), CD3 (MAb MM1A), CD4 (MAb CACT 138A), CD8 (MAbs CACT 80C and BAT 82B), and the  chain of the / T-cell receptor (TcR) (MAb CACT 61A). These MAbs were kindly provided by William C. Davis, Washington State University, Pullman, Wash.

Detection of IFN- and IL-2 in supernatants of LNC and T-cell lines. Fresh LNC were cultured for 96 h in complete medium with 5 µg of A. marginale membrane antigen per ml, and supernatants were collected at 72 (first set of calves) or 96 h. T-cell lines were established from cryopreserved, antigen-draining LNC of calves in groups II and III by weekly stimulation with membrane antigen and APC. After 3 weeks, the cells were washed and cultured for 48 h at a density of 2 × 10⁶ cells per ml with 2 × 10⁶ APC per ml and 3 µg of membranes prepared from the Florida strain of A. marginale per ml. Supernatants were harvested by centrifugation and stored frozen at 20°C. The bovine IFN- assay was performed with a commercial ELISA kit (BOVIGAM; CSL Limited, Parkville, Victoria, Australia) according to the manufacturer's protocol. The IFN- activity in culture supernatants diluted 1:5 to 1:2,000 was determined by comparison with a standard curve obtained with a supernatant from a Mycobacterium bovis purified protein derivative-specific Th cell clone that contained 440 U of IFN- per ml (previously determined by the neutralization of vesicular stomatitis virus [8]). In our assay, 0.6 U corresponds to 1 ng of IFN- (2). The results are presented in units or nanograms of IFN- per milliliter. The IL-2 bioassay was performed as described previously (48) in triplicate with supernatants diluted 1:2 with an IL-2-dependent bovine CD8⁺ T-cell clone (G4.3D1) for responder cells and recombinant human IL-2 (Boehringer Mannheim) as a standard. The results are presented in picograms of IL-2 produced per milliliter of cell supernatant.

Analysis of neutralizing antibody against human IL-12. Heat-inactivated sera obtained from calves before and following the third inoculation of MSP-2 and IL-12 were serially diluted from 1:200 to 1:64,000 and tested for neutralization of human IL-12. An IL-12 bioassay based on induction of IFN- by IL-12- and phytohemagglutinin (PHA)-stimulated PBMC was used (42). Diluted sera were incubated with 0.02 ng of IL-12 at 37°C for 1 h and then added along with 1 µg of PHA (Sigma Chemical Co.) to 2 × 10⁶ PBMC cultured in 1 ml of complete medium. Supernatants were harvested 48 h later and tested for IFN- by ELISA. At dilutions of 1:200 or greater, preimmunization sera had no inhibitory activity. As a positive control, serial dilutions of goat anti-human IL-12 IgG (R & D Systems, Minneapolis, Minn.) were also mixed with 0.02 ng of IL-12 and tested for induction of IFN-, and the dose that neutralized 50% of the biological activity (ND₅₀) was 0.5 µg.

QC-RT-PCR analysis of cytokine transcripts in the LNC from immunized calves. As ELISA-based assays to quantify bovine IL-4 and IL-10 are not commercially available, quantitative, competitive reverse transcription-PCR (QC-RT-PCR) analysis of cytokine mRNA was performed. RNA was prepared from antigen-draining and contralateral prescapular LNC from all calves prior to or following culture for 6 or 12 h of 2.7 × 10⁶ cells per ml with 5 µg of A. marginale membrane antigen per ml. Total cellular RNA was extracted using the Trizol reagent (GIBCO-BRL, Gaithersburg, Md.), and RNA samples were stored at 80°C. QC-RT-PCR was performed as described previously (48-50), with minor modifications. Briefly, competitor molecules (mimics) for bovine IL-2, IL-4, IL-10, and IFN- were kindly provided by Dante Zarlenga (Department of Immunobiology and Disease Resistance, U.S. Department of Agriculture, Agriculture Research Service, Beltsville, Md.), and the bovine -actin mimic was generated in our laboratory as described by Zarlenga et al. (52). The primer sequences used to amplify the cytokine cDNAs were exactly as described previously (48-50), with the exception of the IL-2 reverse primer, for which the correct sequence is 5' TCA AGT CAT TGT TGA GTA GAT GCT T 3'. The resultant IL-2, IL-4, IL-10, IFN-, and -actin competitor PCR fragments were distinguishable from native fragments by their smaller size (48, 50). Column-purified, RNA-free plasmids containing cytokine competitors were serially diluted 10-fold with sterile double-distilled water and stored at 20°C until used. Total RNA (0.5 to 1.0 µg) was reverse-transcribed to cDNA in a 20-µl volume by using oligo(dT)₁₆ (Perkin Elmer, Branchburg, N.J.) according to the manufacturer's instructions. For each sample tested, PCRs were performed, with each reaction mixture containing PCR primers; mimic DNA (0.1 to 1000 fg); cDNA (0.05 to 5 ng); a master mixture containing 10× PCR buffer (final concentration, 1×), magnesium (final concentration, 2.5 mM), and deoxynucleoside triphosphates (final concentration, 1 mM); AmpliTaq-Gold (1 U per reaction mixture; Perkin-Elmer); and water in a 50-µl volume. The PCR mixture was preheated to 94°C for 10 min to activate the AmpliTaq-Gold, followed by 35 cycles of amplification under the following conditions: 94°C for 1 min, 60°C for 1 min, and 72°C for 2 min. The reactions were completed by an extension at 72°C for 10 min and stored at 4°C until analyzed. PCR products (20 µl) were electrophoresed on a 1% agarose gel containing ethidium bromide and quantified under UV light using a digital imaging system (IS1000; Alpha Innotech Corporation, San Leandro, Calif.). After correcting for differences in molecular weight between native and competitor DNA, the ratios between the amplified products of the target and competitor sequences at each competitor concentration were calculated. The logs of the ratios were plotted against the input concentrations of competitor DNA, and a regression equation was obtained. At the point of equivalence, where the amplified target/competitor DNA ratio equals 1.0, the amount of cytokine cDNA in the test sample equals the amount of competitor DNA. To compare the amount of cytokine mRNA in different samples, cytokine mRNA levels were normalized to the amount of -actin. Genomic DNA was not detected for any cytokine or -actin in the RNA samples. Results are presented in femtograms of cytokine RNA per microgram of total cellular RNA.

Statistical analysis. A one-tailed, nonpaired Student's t test was used to compare the mean levels of proliferation, IFN- production, and steady-state cytokine transcript levels in LNC for the groups of calves. A one-tailed, paired Student's t test was used to compare these parameters for right and left prescapular LN in the different groups. A P value of 0.05 was considered significant.

	RESULTS

Top Abstract Introduction Materials and Methods Results Discussion References

A. marginale-specific proliferation in PBMC of MSP-2-immunized calves. Calves were immunized, as detailed in Table 1, at 3- to 4-week intervals with gel-purified native MSP-2 antigen in alum and with or without IL-12 until specific proliferation was observed. PBMC were tested after each immunization for proliferation against several concentrations of membrane antigen prepared from A. marginale (Florida strain) or control URBC. Calf 61, which received MSP-2 and IL-12, responded after the third inoculation, whereas the remaining calves in both immunized groups did not respond until after the fifth antigen inoculation, at 17 or 18 weeks. The responses were variable, with those of calves 63 and 59 being the weakest (Fig. 2). Control calves that did not receive MSP-2 failed to respond to A. marginale or URBC at any time point (data not shown).

View larger version (23K): [in this window] [in a new window]   FIG. 2.   Dose-dependent, antigen-specific proliferative responses of PBMC from MSP-2-immunized calves. PBMC were obtained at 2 (calves 57, 60, 61, 63, and 65) or 3 (calf 59) weeks following the fifth antigen inoculation and tested for proliferation against 0 to 25 µg of membrane antigen prepared from A. marginale or URBC per ml. Cells were cultured for 6 days, radiolabeled, harvested, and counted on a scintillation counter. Data are the means ± the SEM of triplicate cultures. For the response to 25 µg of A. marginale per ml, SI values are also indicated.

IgG responses in calves immunized with MSP-2 or MSP-2 and IL-12. Serological responses were monitored throughout the immunization by Western blot analysis. All preimmunization sera and control sera from calves immunized with alum and IL-12 were negative for reactivity on the immunoblots (data not shown). IgG responses in all three calves that received IL-12 and MSP-2 were detected at the first time point tested, 2 weeks following the second antigen inoculation (week 6), whereas only one of three calves inoculated with MSP-2 alone was seropositive (data not shown). The other two calves in the MSP-2 only group seroconverted after the third (week 10) and fourth (week 13) antigen injections. The sera reacted with a 36-kDa band on the immunoblots, which coincides with the molecular mass of MSP-2. Analysis of IgG1- and IgG2-specific titers in sera obtained 2 weeks after the fifth inoculation of antigen showed that the calves immunized with IL-12 made significantly more IgG1 than the calves that received MSP-2 alone (Table 3). Furthermore, one of three calves in the IL-12 group produced IgG2.

Analysis of antigen-induced proliferation and cytokine production by draining LN lymphocytes. Once A. marginale-specific proliferative and serological responses were detected, the calves were given a final antigen inoculation so that antigen-draining (right) and contralateral (left) lymph nodes could be surgically biopsied for examination of antigen-induced recall responses. The booster inoculation was staggered so that one calf from each group was used for each of three time points (Table 1). The relative percentages of T-cell subsets in the LN were similar in all groups (Table 4).

View larger version (28K): [in this window] [in a new window]   FIG. 3.   Comparison of the A. marginale-specific proliferative responses of antigen-draining (right) and adjuvant control (left) LNC from control and MSP-2-immunized calves. Cell suspensions were obtained from left and right prescapular LN biopsies of one calf per group at three different times. Freshly obtained (A, B, D, E, G, and H) or cryopreserved (C, F, and I) LNC from the antigen-draining right LN or adjuvant control left LN were assayed for proliferation against 0 to 25 µg of A. marginale or control URBC per ml (data not shown). LNC (3 × 105) were cultured for 4 days, radiolabeled, harvested, and counted. Data are the means ± the SEM of triplicate cultures and are representative of three separate assays performed with fresh or cryopreserved LNC.

View larger version (11K): [in this window] [in a new window]   FIG. 4.   Comparison of IFN- and IL-2 production by LNC from calves immunized with MSP-2 or MSP-2 and IL-12. Freshly obtained LNC were cultured for 24 to 96 h at a concentration of 2.7 × 106 cells per ml with 5 µg of A. marginale membrane antigen per ml. Supernatants were collected, centrifuged, and tested for IFN- by ELISA (A) or for IL-2 by bioassay and an IL-2-dependent T-cell clone (B). Results for individual cattle are indicated by the shaded bars. Results for IFN- are the amounts of IFN- produced in 72-h (calves 61, 62, and 65) or 96-h (all other calves) supernatants (data are means + SEM [error bars] of the results of duplicate assays per sample) and are based on a standard curve obtained with bovine IFN-. Results for IL-2 are the amounts of IL-2 produced in 48 h supernatants (values are means ± SEM) based on assays of triplicate wells per sample and a standard curve obtained with human IL-2.

Cytokine transcript expression by antigen-draining and contralateral LNC. To verify the adjuvant effect of IL-12 on enhancing IL-2 and IFN- production and to examine other cytokines important for priming and immune regulation, QC-RT-PCR analysis of IL-2, IFN-, IL-4, and IL-10 transcript expression was performed with RNA obtained from LNC of all calves. RNA was obtained from freshly collected LNC or following stimulation with A. marginale for 6 or 12 h. In MSP-2-immunized calves, the amount of cytokine transcript determined by RT-PCR increased following antigen activation (data not shown), so RNA from the 12-h time point was selected for use in QC-RT-PCR. For both MSP-2-immunized groups, comparison of the mean transcript levels in antigen-draining (right) LNC and contralateral (left) LNC revealed higher transcript levels in the antigen-draining LNC (Fig. 5). Calves given MSP-2 and IL-12 (group III) had the highest mean levels of transcripts in both antigen-draining (right) and contralateral (left) LNC. When the mean levels of transcripts were compared, group III calves had approximately ninefold more IL-2 and fourfold more IFN- than the calves immunized with MSP-2 alone (group II). Although the difference in IFN- transcript levels between group II and III calves was not significant due to the low response of calf 59, calves 60 and 61 had IFN- transcript levels well above 95% confidence limits of the mean IFN- values for group II calves. IL-4 and IL-10 transcripts were absent or were present at levels that were relatively low in all calves but higher in the group III calves than in group II calves. Overall, the relative steady-state levels of IL-2 and IFN- transcripts analyzed using QC-RT-PCR were consistent with the relative amount of cytokine product determined by bioassay or ELISA. Collectively, these data demonstrate that immunization with IL-12 augments the production of IL-2 and IFN- during a recall response to antigen.

View larger version (15K): [in this window] [in a new window]   FIG. 5.   QC-RT-PCR analysis of cytokine mRNA levels following antigen stimulation of antigen-draining (right) and control contralateral (left) prescapular LNC. LNC were obtained from one animal per group 3 days following the final MSP-2 inoculation. Freshly obtained LNC (2.7 × 106 per ml) were cultured for 12 h with 5 µg of A. marginale membrane antigen per ml, and RNA was prepared. QC-RT-PCR analysis was performed for -actin and cytokines IL-2, IFN-, IL-4, and IL-10, and the amount of transcript was calculated, as described in the text, based on the known amount of cytokine competitor gene added. The data are plotted for individual animals in groups I (IL-12 and alum), II (MSP-2 and alum), and III (MSP-2, IL-12, and alum), respectively: calves 56, 57, and 59 (squares); calves 62, 63, and 60 (circles); and calves 58, 65, and 61 (triangles). The mean LN cytokine transcript levels for each group are indicated by the horizontal lines.

Neutralizing antibody to human IL-12. The variable cytokine responses among calves immunized with MSP-2 and IL-12 (Fig. 4 and 5) raised the possibility that the differences might correlate with the presence of neutralizing antibodies to human IL-12. By an IL-12 bioassay consisting of costimulation of bovine PBMC with 0.02 ng of IL-12 and 1 µg of PHA, which stimulated production of approximately 150 U of IFN- per ml (data not shown), serially diluted bovine sera had ND₅₀ titers of 2,506 (calf 59), 2,512 (calf 60), and 1,932 (calf 61). Thus, although three immunizations of human IL-12 did elicit neutralizing antibodies to human IL-12, the ND₅₀ titers did not correlate with the different levels of cytokine expression among group III calves.

Antigen-induced proliferation and IFN- production by short-term T-cell lines established from antigen-draining LNC. We next wished to determine if effector cells cultured from the antigen-draining LN maintained the type 1 cytokine phenotype for several weeks. Short-term T-cell lines were established from all three group III calves and from group II calf 63 by weekly stimulation of LNC with A. marginale membrane antigen and APC. We were unable to establish vigorously growing cell lines from group II calves 57 and 65, so after the 3-week culture period, only enough cells were available to test for IFN- production. The inability to propagate cells from these animals is consistent with the low or absent proliferation of these LNC (Fig. 3). All four cell lines that were expanded were comprised mainly of CD4⁺ T cells (93 to 95%). In proliferation assays these four cell lines responded similarly to A. marginale, after 1 to 3 weeks of culture (data not shown). However, cell lines from MSP-2- and IL-12-immunized calves produced significantly more IFN- (Table 5).

View this table: [in this window] [in a new window]   TABLE 5.   IFN- production by T-cell lines established from calves immunized with A. marginale MSP-2 without or with IL-12

Duration of the memory response to A. marginale. To determine if immunization with MSP-2 and IL-12 elicited long-term immunological memory, PBMC obtained from all six MSP-2-immunized calves 9 months after the last group was boosted with MSP-2 were tested for antigen-specific proliferation. Dose-dependent and specific responses to A. marginale homogenate were observed in two MSP-2-immunized and all three MSP-2- and IL-12-immunized calves, with the highest responses observed in calves that received IL-12. The SI values in response to the optimal antigen concentration (5 or 25 µg of protein per ml) for group II calves 57, 63, and 65 were 2.6, 3.1, and 1.3, and those for group III calves 59, 60, and 61 were 4.6, 3.6, and 27.7, respectively, which values are representative of two experiments. The lack of response by PBMC from calf 65 is consistent with the lack of a recall response in the antigen-draining LNC (Fig. 3).

	DISCUSSION

Top Abstract Introduction Materials and Methods Results Discussion References

This study is the first to examine CD4⁺ T-cell responses in cattle immunized with native MSP-2 antigen. We demonstrated specific and long-lived recognition of purified A. marginale membranes or organism homogenate from the homologous Florida strain by CD4⁺ T cells from PBMC and LNC, showing that MSP-2 is capable of priming for an anamnestic T-cell response to the organism. These data are consistent with earlier studies which showed that PBMC and several CD4⁺ T cell clones obtained from calves immunized with purified A. marginale membranes responded to organism homogenate, purified outer membranes, and MSP-2 (7, 9). MSP-2 and related proteins, including the OMP of C. ruminantium (MAP 1), E. chaffeensis (OMP-1), and the agent of HGE (GE MSP-2 and HGE-44), are candidate vaccine antigens (28, 30, 31). Our results are thus directly relevant for the potential use of ehrlichial OMP as immunogens for ehrlichial pathogens of humans and domestic animals (14, 18, 27, 28, 30, 36, 51, 53).

The requirement for five immunizations to detect antigen-specific proliferation is likely due to the use of alum, which is a poor adjuvant. When either RIBI or complete Freund's adjuvant was used with a comparable amount of protein antigen from Babesia bigemina (37) or A. marginale (MSP-1) (W. C. Brown, T. C. McGuire, and G. H. Palmer, unpublished observations), specific proliferative responses were detected after three antigen inoculations. Additionally, when cattle were immunized with A. marginale membranes in saponin, responses were detected after two or three inoculations (7).

This study also demonstrates the adjuvant effect of IL-12 in priming for enhanced memory IgG and type 1 cytokine responses to A. marginale MSP-2. Alum was used with IL-12, since in mice alum fails to elicit a type-1 response, permitting an evaluation of the effects of IL-12, and because it appeared to prolong the in vivo effect of IL-12 (19). IL-12 promotes type-1 responses in several ways (reviewed in reference 16). First, IL-12 produced by the major APC, the dendritic cell, acts on naïve Th cells during antigen priming, causing them to differentiate into Th1 cells that secrete high levels of IFN- upon stimulation. Second, as a costimulator, IL-12 potentiates the secretion of IFN- by differentiated T cells in response to specific antigen. Finally, IL-12 stimulates the differentiation of IFN--producing effector cells from memory cells when cultured with the priming antigen. Our studies with bovine CD4⁺ T cells have also shown the ability of IL-12 to enhance IFN- production by antigen-stimulated Th0 and Th1 clones, and to promote the differentiation of IFN--producing effector cells from resting PBMC-derived lymphocytes that were subsequently cultured for several weeks with antigen (4, 49). However, the results presented here are the first to demonstrate the in vivo effects of administering IL-12 to cattle as an adjuvant for a soluble protein antigen.

The effects of using IL-12 as an adjuvant during immunization with MSP-2 were evaluated only after multiple immunizations, so that immediate effects on priming were not determined. Instead, our experiments examined the effect of IL-12 on a recall response. As expected, IL-12 stimulated significantly higher production of IFN- by LNC draining the MSP-2 injection site and by short-term cultured CD4⁺ T-cell lines established from these cells. The production of IFN- by the CD4⁺ T-cell lines indicates that CD4⁺ T cells are a source of IFN- in the LNC. Five- to tenfold more IFN- was produced by these cell lines than by the CD4⁺ T-cell line established from calf 63 immunized with MSP-2 alone, or by CD4⁺ T cell lines from two calves immunized with A. marginale outer membranes in saponin (7). These results are consistent with the previously observed effects of IL-12 on differentiated T-cell clones and on memory T cells cultured with IL-12 and antigen (4, 49).

Elevated expression of IL-2, IL-4, and IL-10 was also observed in the IL-12 and MSP-2-immunized calves, demonstrating that IL-12 did not polarize the response to a strictly Th1 response. IL-10 was similarly induced by IL-12 following priming in mice or in vitro priming of human T cells, presumably as a negative-feedback response (16). Furthermore, immunization with IL-12 supported the development of both Th1 and Th2 recall responses to keyhole limpet hemocyanin in mice (3). These mixed Th1 and Th2 cytokine responses were accompanied by mixed IgG2a and IgG1 responses. Additionally, the response to a soluble protein antigen adsorbed with alum was shifted from a Th2-biased response, characterized by predominant IL-4, IL-5, and IL-10 cytokine and IgG1 antibody responses, to a Th1 response, marked by increased IFN-, decreased IL-4, IL-5, and IL-10 responses, and induction of IgG2a, IgG2b, and IgG3 (19). However, significantly increased IgG1 titers were observed in the IL-12-treated mice, suggesting that the regulation of IgG1 in this system was independent of IL-4.

In cattle, IFN- enhanced IgG2 production and IL-4 enhanced IgG1 production by B cells activated through T-independent type 2 stimulation (10, 11). Furthermore, the production of IFN- by CD4⁺ T-cell clones cultured with antigen and B cells correlated with IgG2 production by the B cells (6). Based on this information, we expected to stimulate only IgG1 production with MSP-2 and alum, and both IgG1 and IgG2 antibody responses with the combined IL-12-MSP-2-alum formulation. Although a restricted IgG1 response in calves given MSP-2 alone occurred and addition of IL-12 enhanced this response, IL-12 had no consistent effect on IgG2 production. There are several possible explanations for this result. First, the amount of IL-12 used (three inoculations of 10 µg) may have been too little in this large animal species to induce sufficient IFN- in vivo to facilitate isotype switching. Second, the development of neutralizing antibodies against human IL-12 may have prevented the optimal induction of bovine IFN- and suggests that it would be preferable to use homologous IL-12. Finally, in cattle, T-cell-dependent IgG2 production may not be solely dependent on IFN-. In support of the latter possibility, Estes et al. (12) recently demonstrated that when bovine B cells were costimulated with IL-2, CD40 ligand and anti-surface IgM to mimic T-cell-dependent activation, the addition of IFN- enhanced IgG2 production only twofold, whereas type-1 IFN had a greater effect. Furthermore, in our study the single calf (calf 59) that produced IgG2 was the lowest responder in terms of PBMC proliferation and LNC IL-2 and IFN- production, again suggesting that factors other than or in addition to IFN- are important for IgG2 production.

Enhanced IL-2 production, which was associated with higher levels of transcript expression and significantly greater proliferation by antigen-draining LNC, was demonstrated in calves that received IL-12. This result contrasts that of Jankovic et al. (19), who observed an IFN-- and NO-dependent suppression of IL-2 production and antigen-induced proliferation of splenocytes from mice immunized with IL-12 and antigen coadsorbed to alum. The suppression was dependent on the dose of IL-12, which supports the possibility that the amount of IL-12 given in our experiments was not sufficient to induce suppressive levels of IFN-. Toxicity with high doses of IL-12 has been observed in mice and humans (22), but the dosage and timing of IL-12 administration used in our experiments did not cause inhibition of bovine lymphocyte responses.

The choice of IL-12 as an adjuvant to induce protection against acute infection with ehrlichial pathogens, such as A. marginale, is supported by our results. Although the calves in this study were not challenged, the strong IFN- response by T-cell lines from calves protectively immunized with A. marginale outer membranes is consistent with our hypothesis that protection is in part dependent on IFN- production (7, 34). Furthermore, experiments in mice with related rickettsial organisms demonstrated the importance of IFN- and NO in the protective immune response (13, 23, 35). Protection against ehrlichial pathogens may also be mediated by cytophilic antibodies that can facilitate phagocytosis and killing of the organisms. In cattle both IgG1 and IgG2 subclasses are capable of in vitro binding to activated macrophages, but only IgG2 had opsonizing activity for monocytes and neutrophils, suggesting that this subclass may be more important for phagocytosis in vivo (25). Although it is still uncertain how bovine IgG2 responses to T-cell-dependent antigens are regulated in vivo, IL-12 should enhance macrophage activation through the induction of IFN- and aid in clearance of the infection caused by A. marginale and related organisms.