INTRODUCTION

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Bovine tuberculosis, a zoonotic disease caused by infection with Mycobacterium bovis (45), is a major economic problem in a number of countries (12) and a serious public health risk in others (18). While a spectrum of immune responses to bovine tuberculosis has been characterized (45, 54), it is generally accepted that protective immunity is mediated through the cellular immune system. A detailed understanding of these responses is essential for the development of better control methods.

It has been suggested that all major T-cell subsets are involved in immune responses to mycobacteria (6, 31, 43). Studies involving experimental Mycobacterium tuberculosis infection, including gene deletion mutations and adoptive transfer experiments in the murine model, have shown that both and T cells have roles in such immune responses (35, 49, 51). To date, much attention has focused on T-cell functions, but there has been increasing evidence that human and murine T cells become potently stimulated by various mycobacterial antigens, including heat shock (24, 48) and other protein antigens (5, 9), along with nonpeptide phosphate-rich low-molecular-weight compounds (17, 20, 57).

In the ruminant system, T cells constitute up to 75% of peripheral blood mononuclear cells (PBMC) in young animals (40) and up to 40% of the circulating population in adults (15, 41, 60). In contrast, only 7% of human PBMC and 2 to 3% of murine PBMC typically express the T-cell receptor (TCR1) (10, 30). Furthermore, a unique feature of ruminant T cells is the expression of a 215-kDa surface molecule identified as WC1 on the majority of TCR1⁺ PBMC (15, 42, 61). The extracellular portion of this molecule has 11 repeats of a cysteine-rich domain and belongs to the scavenger receptor cysteine-rich family of proteins, which also includes CD5 and CD6 (61). It has been suggested that WC1 is a possible ligand for E-selectin (59) and that it may control the tissue-specific homing of T cells (62). More recently, it has been proposed that WC1 regulates interleukin-2 (IL-2)-dependent T cells and their proliferation through induction of reversible growth arrest (34, 56). However, the precise functions of this molecule and indeed of T cells are still not clearly defined.

Given the apparent role of T cells in human and murine tuberculosis, the greater numbers of these cells found in ruminants suggest that they could have an important role in bovine tuberculosis, which requires further investigation. A range of functions, including proliferation and natural killer and cytotoxic activity, have been documented for bovine T cells in response to mitogens and parasite, bacterial, and viral antigens (1, 14, 15, 16, 19), and it is likely that such functions could be involved in the defense against M. bovis. Furthermore, it has previously been demonstrated that the WC1⁺ cells are among the first T cells to show changes in circulating numbers and antigen responsiveness following experimental M. bovis infection of cattle (53).

The aim of the present study was to investigate the in vitro responsiveness of T-cell subsets to mycobacterial antigens using a model of bovine tuberculosis established in the natural host.

	MATERIALS AND METHODS

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Experimental animals. Two groups of Friesian cross, male calves (approximately 6 months of age) obtained from herds with no history of M. bovis infection for at least 5 years were used in this study. All animals were screened for lymphocyte proliferation and for gamma interferon (IFN-) production against a range of M. bovis and control antigens to confirm disease-free status. Animals were selected on the basis of a negative response to M. bovis antigens and low reaction with Mycobacterium avium. Group 1 contained three experimentally infected (I1, I2, and I3) calves and three uninfected age-matched controls (U1, U2, and U3). Group 2 contained four experimentally infected animals (I4, I5, I6, and I7) and two uninfected animals (U4 and U5). Animals for experimental infection were inoculated with 10⁶ CFU of a field strain of M. bovis (T/91/1378) by intranasal instillation and housed in strict isolation (44). Animals were sampled at weeks 3 to 10 for lymphocyte functional studies and were confirmed as diseased by gross postmortem examination (weeks 40 to 41 postinfection [p.i.]) and M. bovis culture.

Mycobacterial antigens. M. bovis sonic extract (MBSE) was prepared as previously described (52). Briefly, M. bovis (T/91/1378) was grown to mid-log phase in Middlebrook 7H9 medium. Bacteria were harvested by centrifugation, washed in phosphate-buffered saline (PBS) and subjected to ultrasonication. MBSE was clarified by centrifugation, filter sterilized (0.22-µm-pore-size filter), and stored at 70°C. M. bovis culture filtrate (CF) was prepared by culturing M. bovis (T/91/1378) in Sauton's specific protein-free medium for 21 days at 37°C in air. Bacteria were removed by centrifugation, and the supernatant was filter sterilized and concentrated 100-fold by gas pressure in an ultrafiltration cell containing a 10-kDa-cutoff membrane (Amicon Ltd., Stonehouse, Gloucestershire, United Kingdom).

Antibodies. Monoclonal antibodies (MAbs) CC8 (anti-CD4), CC63 (anti-CD8), CC15 (anti-WC1; isotype, immunoglobulin G2A [IgG2a]), and CC30 (anti-CD4; isotype, IgG1) (26, 28, 42), obtained from the European Collection of Animal Cell Cultures (Porton Down, Wiltshire, United Kingdom), were prepared as hybridoma culture supernatants and used at 1/10 dilution for flow-cytometric analysis (FCA) and magnetic (magnetically activated cell sorting [MACS]) labeling. GB21A (anti- TCR/TCR1; isotype, IgG2b) and CACT116A (anti-CD25/IL-2R; isotype, IgG1) (38, 39) purified antibodies were obtained from Veterinary Medical Research and Development Inc. (Pullman, Wash.) and used at 1/100 dilution for FCA labeling. For flow cytometry, primary MAbs were detected using secondary goat anti-mouse (GAM) isotype-specific conjugates (IgG2a-fluorescein isothiocyanate [FITC], IgG2b-FITC, IgG2b-biotin, and IgG1-phycoerythrin [PE]). The GAM-IgG2b-biotin was detected using streptavidin-SpectralRed (Southern Biotechnology Associates, Inc., Birmingham, Ala.).

Magnetic purification of CD4⁺ and WC1⁺ T cells. PBMC were separated from heparinized blood samples over Ficoll-Paque as described previously (52). CD4⁺ and WC1⁺ cells were labeled with antibovine MAb CD4 (CC8) or WC1 (CC15) (1/10 dilution) and positively selected with GAM microbeads using the Miltenyi Biotec (Bergisch Gladbach, Germany) MACS system as described previously (36).

Preparation of APC. Isolated PBMC from each animal were resuspended at 10⁷ cells/ml and incubated with mitomycin C (50 µg/ml) (Sigma) at 37°C for 30 min. The antigen-presenting cells (APC) were washed three times with PBS by centrifugation and resuspended in TCM at 10⁶ cells/ml.

Lymphocyte proliferation assay (LPA). Proliferation assays were performed using PBMC or purified T-cell subsets with autologous APC. PBMC were prepared at 10⁶ cells/ml, while purified CD4⁺ and WC1⁺ T cells were resuspended at a concentration of 1.5 × 10⁵ cells/ml with APC added at 10⁵ cells/ml. Cell suspensions (200 µl/well) were dispensed into 96-well, flat-bottom microtiter plates (Nunc, Roskilde, Denmark). Antigens were added to triplicate wells at a previously determined optimal concentration (4 µg/ml), and an equal volume of PBS was added to control wells. The cultures were incubated for 5 days, pulsed with 0.25 µCi of [³H]thymidine (Amersham International, Amersham, United Kingdom), and harvested, and the incorporated radiolabel was measured by liquid scintillation as previously described (52) and recorded as counts per minute. Results are expressed as either mean total counts per minute or mean net counts per minute (net counts per minute = antigen counts per minute  control PBS counts per minute).

Detection of in vitro activation of T cells by FCA. Cultures were established for each animal to determine the phenotype of T cells becoming activated in the presence of an antigen. PBMC were resuspended at 10⁶ cells/ml in TCM, and 7-ml cultures were maintained in 25-cm² tissue culture flasks (Costar Corp., Cambridge, Mass.). Cultures were stimulated with MBSE (4 µg/ml) or an equivalent volume of PBS (control) and incubated in 6% CO₂ at 37°C. After specified periods, cells from PBMC cultures were harvested and labeled for two-color (CC8, CC63, or CC15 and CACT116A) and three-color (CC15, GB21A, and CACT116A) FCA. Cells (10⁶ per test) were pelleted in U-well microtiter plates, resuspended in 25 µl of MAbs diluted in PBS containing 10% (vol/vol) heat-inactivated normal rabbit serum (PBS-NRS), and incubated for 30 min at 4°C. The cells were washed twice in PBS containing 0.1% (wt/vol) sodium azide (Sigma). Cells were then resuspended in 25 µl of the appropriate GAM isotype-specific conjugates (IgG2a-FITC, IgG1-PE, IgG2b-biotin; used at 1/500 in PBS-NRS), incubated, and washed as described above. For tertiary labeling of IgG2b-biotin, cells were incubated with 25 µl of streptavidin-SpectralRed (1/500 in PBS-NRS). Following final washes, cells were fixed in 400 µl of 1% (wt/vol) paraformaldehyde (Sigma) in PBS.

IFN- enzyme-linked immunosorbent assay. Cultures of PBMC or T-cell subsets (CD4⁺ or WC1⁺) with autologous APC were set up as for LPA above with the PBS control or M. bovis antigens. Following 96 h of incubation, 100 µl of supernatant was aspirated from duplicate wells and assayed for IFN- using an enzyme immunoassay (Commonwealth Serum Laboratories Ltd., Parkville, Victoria, Australia), performed as specified by the manufacturer. Results were expressed as optical densities at 450 nm (OD₄₅₀) or OD indices (ODI) (37) (ODI = OD for the antigen/OD for the PBS control). An ODI of >2 and also greater than the ODI for APC controls was considered positive.

Statistical analysis. The interaction between infection status (where applicable) and the effects of PBS or MBSE on the activation status within each T-cell subset as measured by two-color FCA, proliferation, and IFN- release following culture was investigated by analysis of variance using GENSTAT statistical software (Clarendon Press, Oxford, United Kingdom).

	RESULTS

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Antigen-specific CMI responses in M. bovis-infected cattle. From 21 days after experimental infection, group 1 animals (I1, I2, and I3) had consistent cell-mediated immune (CMI) responses to MBSE and CF as measured by LPA and IFN- release, while the three noninfected control cattle (U1, U2, and U3) did not show significant responsiveness (Table 1). During the initial stages of this response, FCA was used to analyze the in vitro antigenic activation status of T-cell subsets by measuring the expression of IL-2R (CD25).

View this table: [in this window] [in a new window]   TABLE 1.   Antigen responsiveness of PBMC from uninfected and M. bovis-infected animals stimulated with control or M. bovis antigens as measured by lymphocyte proliferation and IFN- production from 21 to 63 days p.i.a

In vitro activation of T-cell subsets. Initially, cultures of PBMC from the animals of group 1 were stimulated with PBS (control) or MBSE for 24 h prior to FCA. As Fig. 1 demonstrates, distinct levels of T-cell subset activation were observed in response to MBSE, with a high degree of activation within the CD4⁺ and WC1⁺ populations of the infected animals. A relatively low degree of CD25 expression on CD8⁺ T cells was observed.

View larger version (61K): [in this window] [in a new window]   FIG. 1.   Representative two-color flow-cytometric dot plots of phenotype (CD4+ or WC1+; FL1) and CD25 (IL-2R) expression (FL2) of PBMC from an individual M. bovis-infected animal following 24 h of culture with PBS (control; a and b) or MBSE (c and d). Percentages of cells with the subset phenotype activated (upper right) were calculated by dividing the percentage of CD4+ (or WC1+) CD25+ cells by the percentage of CD4+ (or WC1+) cells and multiplying by 100.

View larger version (27K): [in this window] [in a new window]   FIG. 2.   Proportions of activated (CD25+) and nonactivated (CD25) CD4+, CD8+, and WC1+ T-cell subsets within the total lymphocyte gated population as determined by FCA of uninfected (a) and M. bovis-infected (b) animals following 24 h of culture with PBS (Cont) or MBSE. Results are means ± standard errors of the means for three uninfected and three infected cattle (group 1). Experiments were repeated on five occasions. Statistical comparisons between PBS control and MBSE cultures for the proportion of activated cells within each T-cell subset are shown (**, P < 0.01; ***, P < 0.001.

Kinetics of in vitro activation of T cells. The analysis of T-cell subset activation at 24 h of culture for group 1 infected animals showed the predominant involvement of CD4⁺ and WC1⁺ cells. This was also found to be the case with animals of group 2 from as early as 28 days p.i. (data not shown). Subsequently, time course analysis was performed with the group 2 infected animals to define the kinetics of T-cell subset activation in vitro from 0 to 168 h following stimulation with MBSE.

View larger version (30K): [in this window] [in a new window]   FIG. 3.   Kinetics of and T-cell activation. Shown are percentages of T-cell subsets coexpressing CD25 as determined by FCA at various times after 0 to 168 h of culture with PBS (Cont) or MBSE. Results are means ± standard errors of the means for four M. bovis-infected cattle (group 2). Statistical comparisons between control and MBSE cultures at each time point revealed the first significant differences in activation at 18 ( T cells; P < 0.05; a and d) and 24 h ( T cells; P < 0.01; b and c). Beyond 24 h, significant activation of CD4+ (a) cells was apparent up to 144 h (P < 0.01 or P < 0.001), significant activation of CD8+ cells was apparent at 48 h only (P < 0.05) (d), and significant activation of T cells (TCR1+ and WC1+) was apparent at all time points (P < 0.01 or P < 0.001) (b and c).

Differential antigen responsiveness of WC1⁺ and WC1 T cells. The kinetics study revealed that the activation profile of the TCR1⁺ (total T-cell) population was mirrored by the activation profile of the WC1⁺ subset (Fig. 3b and c) suggesting a possible relationship between WC1⁺ expression and activation. Three-color FCA of T-cell subset phenotype and activation status following 24 h of culture was performed to investigate coexpression of CD25 and WC1⁺ on TCR1⁺ cells. Data which are representative of the overall mean results from repeated experiments using group 2 infected animals are shown in Fig. 4. The results demonstrate how the main populations of activated (TCR1⁺) T cells in both control and MBSE-stimulated cultures were WC1⁺ (approximately 84%), whereas a much smaller number of nonactivated T cells expressed WC1⁺ (Fig. 4c and f), particularly in MBSE-stimulated cultures. Analysis of the overall data clearly shows that the majority of the predominant population of WC1⁺ cells within M. bovis antigen-stimulated cultures exist in a highly activated state (Table 2), making up a large proportion of the highly activated cells within the total PBMC culture (Fig. 4).

View larger version (66K): [in this window] [in a new window]   FIG. 4.   Expression of WC1 on activated and nonactivated TCR1+ T cells. Shown are representative flow-cytometric dot plots of TCR1 (FL1) and CD25 (IL-2R) expression (FL2) of PBMC from an M. bovis-infected animal following 24 h of culture with PBS (control) or MBSE and corresponding histograms of WC1 expression (FL3). (a) Control (PBS) CD25 versus TCR1 expression dot plot. (b and c) Histograms showing WC1 expression of R2 and R3 gated cells within the dot plot (a), respectively. (d) Dot plot of CD25 and TCR1 coexpression in response to the MBSE antigen. (e and f) Histograms of WC1 expression by cells of gate R2 (e) and gate R3 (f) within the dot plot (d).

View this table: [in this window] [in a new window]   TABLE 2.   In vitro activation (IL-2R expression) of T-cell subsets from M. bovis-infected animals (group 2) following stimulation with MBSE in short-term culture

Functional studies of WC1⁺ and CD4⁺ T cells. The flow-cytometric studies clearly demonstrated that CD4⁺ and T cells from infected animals were highly activated by MBSE. Furthermore, the data suggested that the WC1⁺ subset of T cells was more antigen responsive than the WC1 subset. Thus, CD4⁺ and WC1⁺ T cells were purified by indirect labeling using paramagnetic beads and then cultured with mitomycin C-treated autologous PBMC as APC in order to measure proliferative responses and IFN- secretion in response to M. bovis antigens.

View larger version (17K): [in this window] [in a new window]   FIG. 5.   Proliferation and IFN- release by purified CD4+ or WC1+ T cells and APC only from M. bovis-infected animals in response to MBSE and CF antigens. CD4+ and WC1+ cells were cultured in the presence of autologous mitomycin C-treated PBMC as APC. APC alone were included as controls. (a) Lymphocyte proliferation expressed as mean net counts per minute in excess of control counts per minute (net counts per minute = antigen counts per minute  control PBS counts per minute). (b) IFN- release expressed as ODI (ODI of >2 was considered positive). Results are means ± standard errors of the means for four M. bovis-infected cattle (group 2). Experiments were repeated four times. Results of statistical comparisons between PBS control and MBSE- or CF-stimulated cultures for T-cell proliferation and IFN- production are shown (*, P < 0.05; ***, P < 0.001).

	DISCUSSION

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There has been growing interest in the role of T cells during immune responses, especially in relation to tuberculosis. An increasing body of evidence has shown human and murine T cells responding to mycobacterial antigens (3, 20, 23, 50, 58), possibly displaying many of the effector functions described for T cells (32). The present investigation used a natural host disease model to study the responses of bovine T cells, in comparison with those of T cells, to mycobacterial antigens. The results have indicated a high activation status of bovine in response to M. bovis antigens within this experimental model. The significance of these responses in terms of protective immunity and CMI-based diagnostic tests requires further investigation.

Initial two-color FCA of PBMC T-cell subset activation following 24 h of culture with MBSE revealed powerful activation of CD4⁺ and, in particular, WC1⁺ T cells. While such activation was greatest in infected cattle, it also occurred to a lesser degree in uninfected animals. This was possibly as a consequence of using MBSE, which, like purified protein derivative (PPD), is a very complex mixture of antigens, containing many undefined components. The use of such complex antigens could potentially have resulted in some nonspecific lymphocyte activation in the short-term cultures. Alternatively, the high proportion of WC1⁺ CD25⁺ cells observed in uninfected control animals in response to MBSE (Fig. 2) may suggest a high frequency of precursors within the WC1⁺ population which are capable of responding to M. bovis antigens. There may also be a degree of cross-reactivity with antigens shared with environmental mycobacterial species, resulting in some T-cell activation.

Doherty et al. (21) studied the tuberculin skin reaction in cattle and demonstrated WC1⁺ T cells to be the dominant lymphocyte population in the earliest perivascular infiltrate (6 to 24 h) after intradermal injection of PPD, followed by increasing T-cell infiltration. Early infiltration of - and IL-2R (CD25⁺)-bearing T cells (21) into the skin test site, together with the present findings of rapid activation and proliferation in response to M. bovis antigens, suggests that cells could possibly have a direct or indirect effect on CMI-based diagnostic tests. It may be, for example, that bovine T cells contribute significantly to the development of the skin test response, especially as they may exist in a preactivated state (16) and may become rapidly activated in response to MBSE. Additionally, it has been shown that WC1⁺ cells are involved in recruiting other cells to sites in response to M. bovis antigens (55). However, the exact mechanism by which bovine cells become activated is the subject of ongoing studies.

Following 24 h of culture in the absence of antigens, there was a relatively high level of CD25 expressed by T cells (up to 40%), and it has been reported previously that WC1⁺ cells express CD25 constitutively (16). A ready availability of IL-2R may imply a particular sensitivity to IL-2, and it has been suggested that these cells have a lower threshold for induction of proliferation (34). Thus, there exists the possibility that the level of activation seen within the WC1⁺ population may be partly due to nonspecific stimulation by IL-2 secreted by CD4⁺ cells responding to an antigen(s). Indeed, the present study of the kinetics of in vitro activation indicated that CD4⁺ cells became activated in advance of T cells. Significant CD4⁺ T-cell activation occurred after 12 to 18 h of culture and was followed after 24 h of culture by rises in the level of activation within the total T-cell population (TCR1⁺), mirroring the response profile of the WC1⁺ subpopulation. Previous investigations with sheep have shown that concanavalin A induced maximal activation of CD4⁺ T cells at 24 to 48 h of culture, while WC1⁺ T cells become activated after only 12 h of culture (11). The present observation of a slightly faster rate of activation of CD4⁺ T cells may simply be a feature of the bovine system but may also reflect differences in antigen versus mitogen stimulation.

Elloso et al. (22) demonstrated the human T-cell proliferative response in response to malarial antigens to be dependent on CD4⁺ T-cell secretion of cytokines that signal through IL-2R. In the bovine system it has been reported that purified WC1⁺ T cells require the addition of exogenous IL-2 for proliferation in response to Thileria annulata-infected autologous cells but that IL-2 alone induces a limited WC1⁺ proliferative response (16). Other studies have also reported that IL-2 alone induces minimal proliferation of bovine WC1⁺ cells, implying that IL-2 is required as a secondary signal for activation of cells (15, 29), driving them to proliferation (16). In the present study, the high degree of proliferation of purified WC1⁺ T cells in response to MBSE and CF was observed only in infected animals, indicating the specificity of the response to M. bovis antigens, with a possible requirement for IL-2 and/or other cytokines supplied by other cells. While the mitomycin C-treated PBMC acted as APC and a possible source of cytokines (including IL-2) within the sorted LPA cultures, it should be noted that little IFN- production was detected in APC or WC1/APC cultures from infected animals following stimulation with M. bovis antigen. Although IL-2 levels were not measured within this set of experiments, any activation and proliferation of bovine T cells which were detected following stimulation with M. bovis antigens and influenced by IL-2 are likely to reflect in vivo responses to mycobacterial antigens, where several populations of T cells will be involved. Therefore, results in this paper highlight the activation status of T cells in terms of bovine tuberculosis. Clearly the mechanisms involved in their activation and proliferation and the effect of cytokines influencing their responses (such as IL-2) should be a major area for further investigation, allowing the biological significance of this population of T cells to be fully appreciated.

Interestingly, in the present study both MBSE and CF induced strong proliferation of WC1⁺ T cells. Culture filtrates are known to be rich in immunodominant secretory antigens, which are considered important in early responses (2). Such antigens have been shown to be strong inducers of IFN- production in skin tuberculin test reactor cattle (37). The IFN- pathway is known to be crucial to the development of protective immunity against mycobacteria in mice (33), and, in humans, mutations in the gene for the IFN- receptor result in a much greater susceptibility to mycobacterial infection (46). Here it was observed that CD4⁺ T cells from infected cattle were major producers of IFN- in response to both CF and MBSE, and we have previously shown bovine CD8⁺ cells to be an important source of IFN- in M. bovis infection (36). Human M. tuberculosis-reactive T-cell lines have been observed to produce greater amounts of IFN- than T-cell lines (4). In this study the purified WC1⁺ T-cell cultures from infected animals were found to release small quantities of IFN- in response to the M. bovis antigens. Collins et al. (16) found that WC1⁺ cells did not produce IFN- mRNA, although the message has been observed in bovine T-cell lines (47).

The potent activation and proliferation of WC1⁺ T cells induced by M. bovis antigens demonstrate clearly their involvement in the CMI response to M. bovis, but their role in antimycobacterial immunity remains undefined. It has been demonstrated previously that bovine T cells influence the proliferative responsiveness of CD4⁺ cells in Mycobacterium paratuberculosis infection (14). Other studies have indicated a role for WC1⁺ cells in the modulation of antibody responses (27), and the expression of CD40L on bovine cells may be involved in macrophage activation and may facilitate helper activity in response to B cells (25).

It has recently been suggested that bovine WC1 and WC1⁺ cells represent functionally distinct subsets of T cells which preferentially home to different tissue locations (39). In addition, it has been shown using a SCID-bo mouse model that WC1⁺ T cells play a pivotal, early role in the recruitment of various cell types to sites of M. bovis infection (55). The data presented here indicate that the WC1⁺ population of PBMC form the main population of mycobacterially activated bovine T cells, implying that WC1⁺ expression has an important role in the antigen responsiveness and function of these cells.

Recent reports have suggested that the function of WC1 is to regulate T-cell proliferation through growth arrest (56). This growth arrest was found to correlate with tyrosine phosphatase activation and could be reversed through signalling via the TCR-CD3 complex (34). It was postulated that such a mechanism may control IL-2 responsiveness, while retaining the antigen sensitivity of WC1⁺ T cells (56). WC1 gene families in other species have been described (61), and WC1 expression on porcine T cells has been demonstrated (13). In humans and mice there appear to be WC1 genes, with human genomic WC1 sequences showing 85% homology to those of bovine WC1 (62). However, while T-cell subsets defined by the expression of distinctly rearranged TCRs exist in other species (7, 8), these have not been associated with the expression of any other specific surface molecules. Therefore, as there is no evidence of a human or rodent WC1 homologue, it is possible that bovine T cells (in particular the WC1⁺ cells) have additional, potentially important roles.

In conclusion the results of this study clearly demonstrate that T cells, and in particular the WC1⁺ cells, from M. bovis-infected cattle become highly activated and proliferate strongly in vitro in response to M. bovis antigenic stimulation. Along with previous reports of early infiltration of WC1⁺ cells in response to PPD (21), recruitment of cells to sites of infection by WC1⁺ cells (55), and the influence of WC1⁺ cells on other lymphocyte functions (14, 27), the present findings imply that cells play a central role in immune responses to bovine tuberculosis. While their role in protective immunity requires further investigation, some consideration should also be given to the responses of bovine T cells in response to M. bovis antigens in terms of their influence on the performance of diagnostic tests that are dependent on CMI responses, in particular the skin test. Although purified WC1⁺ cells do not appear to be major producers of IFN-, their influence on the ability of other T cells to produce cytokines and respond to mycobacterial antigens has not yet been fully investigated.