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Infection and Immunity, December 2003, p. 7173-7177, Vol. 71, No. 12
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.12.7173-7177.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.

CD8+-T-Cell Responses of Mycobacterium-Infected Mice to a Newly Identified Major Histocompatibility Complex Class I-Restricted Epitope Shared by Proteins of the ESAT-6 Family

Laleh Majlessi,1* Marie-Jésus Rojas,1 Priscille Brodin,2 and Claude Leclerc1

Unité de Biologie des Régulations Immunitaires, INSERM E352,1 Unité de Génétique Moléculaire Bactérienne, Institut Pasteur, 75724 Paris Cedex 15, France2

Received 23 April 2003/ Returned for modification 10 June 2003/ Accepted 20 August 2003


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ABSTRACT
 
Here we describe the identification of a new CD8+-T-cell epitope, the GYAGTLQSL nonamer, shared by the TB10.3 and TB10.4 proteins of the Mycobacterium tuberculosis ESAT-6 family. Cytotoxic T cells from mycobacterium-infected mice efficiently recognized this epitope. GYAGTLQSL-specific T-cell hybridomas, which were able to recognize Mycobacterium bovis BCG-infected macrophages, were generated and now allow investigation of mycobacterial-antigen processing through the major histocompatibility complex class I pathway.


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TEXT
 
The contribution of CD8+ T cells to the control of infection with Mycobacterium tuberculosis is supported by a marked emergence of gamma interferon-producing CD8+ T lymphocytes in the lungs of infected mice (5, 9, 10) and by the increased susceptibility of mice deficient in genes involved in the major histocompatibility complex class I (MHC-I) presentation pathway to this infection (13). However, the specificity of antimycobacterial CD8+ T cells and the mechanisms of mycobacterial-antigen presentation by MHC-I molecules are poorly understood. Only a few MHC-I-restricted epitopes, i.e., 38-kDa: 225-234 (17), MPT64:190-198 (5), and antigen 85A (Ag85A):144-152 (3) were shown to be recognized by antimycobacterial CD8+ T cells. The MHC-I presentation of mycobacterial antigens maythus be relatively inefficient, and CD8+-T-cell responses to this infection may be induced by substantial expansion of clones with limited specificities (5). Therefore, the identification of MHC-I-restricted mycobacterial epitopes and generation of tools able to detect their presentation in the MHC-I context can be of considerable interest for the investigation of CD8+-T-cell immunity during M. tuberculosis infection.

We applied the SYFPEITHI program (http://syfpeithi.bmi-heidelberg.com/) to 400 open reading frames (ORFs) overlapping the first 10% (Rv0001 to Rv0400) of the M. tuberculosis H37Rv genome (http://genolist.pasteur.fr/TubercuList/) (2). The scan of the first 10% of the genome was performed to obtain a reasonable number of peptides to be synthetized and tested by cytotoxic-T-lymphocyte (CTL) assay. One hundred fifty nonamers which possess consensus H-2Kd-binding motifs were selected. Based on the computed scores of known H-2Kd-restricted peptides, out of these 150 nanomers, only 84 with SYFPEITHI scores of >=23 were considered potentially immunogenic. Moreover, since hydrophobic epitopes may reach an alternative MHC-I pathway (6), we selected only hydrophilous H37Rv peptides (11 out of the 84) (Table 1). As a positive peptide control, we used a previously described H-2Kd epitope, Rv3804c (Ag85A):144-152 (3).


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  		TABLE 1. M. tuberculosis (H37Rv)-derived H-2Kd epitopes predicted by use of the SYFPEITHI algorithm

The selected H37Rv-derived peptides were synthesized by Pepscan Systems (Lelystad, The Netherlands) or Neosystem (Strasbourg, France) and monitored for their capacity to generate CTL responses. BALB/c (H-2d) mice (Iffa Crédo, L'Arbresle, France) received two subcutaneous (s.c.) injections of 50 µg of individual peptides emulsified in incomplete Freund adjuvant at a 2-week interval. Eight days following the last injection, their lymph node cells were stimulated in vitro for 5 days with the homologous peptides and their CTL activity was measured as previously described (4). The Rv0140:79-87 peptide generated only a weak CTL response, while the GYAGTLQSL epitope, shared by the Rv0288 (TB10.4) and Rv3019c (TB10.3) proteins (referred to as TB10.3/4:20-28) and the Rv3804c (Ag85A):144-152 positive-control peptide, elicited CTLs able to efficiently lyse peptide-loaded P815 targets (Fig. 1A). TB10.3 and TB10.4 are low-molecular-weight proteins with 84.4% sequence identity (Fig. 2) and constitute with TB12.9 (Rv3017c) (12) a subfamily of the highly immunogenic ESAT-6 protein family (1, 2, 15). TB12.9 does not share the GYAGTLQSL epitope. It is noteworthy that the actual knowledge of the M. tuberculosis genome does not allow us to precisely anticipate which mycobacterial proteins are secreted. However, among the first 400 ORFs, 6 encode proteins identified in the culture supernatant of M. tuberculosis and 6 others are putatively secreted. Among the ORFs selected here, only TB10.4 and TB10.3 are secreted proteins.



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  		FIG.1. CTL responses to mycobacterial nonamers predicted to bind to H-2Kd. CTL activity in the lymph nodes of BALB/c mice (n = 3) immunized s.c. with individual peptides emulsified in incomplete Freund adjuvant (A), in the splenocytes of mice (n = 4) injected s.c. with 107 CFU of BCG Pasteur 1173P2 (B), or in the splenocytes of mice infected s.c. with 106 CFU of M. tuberculosis (H37Rv) (C) is shown. Eight days after the last injection of H37Rv-derived peptides or 4 weeks after infection with BCG or H37Rv, CTL activity against unloaded or peptide-loaded P815 targets was measured in a standard 5-h 51Cr release assay run in duplicate. The percentage of specific lysis was calculated with the formula 100 x (experimental release - spontaneous release)/(maximum release - spontaneous release). Maximum release was obtained by the addition of 1% Triton X-405 to labeled target cells. Results are representative of at least two independent experiments. Standard deviations were always <5%.



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  		FIG. 2. Alignment of the protein sequences of Rv0288 (TB10.4) and Rv3019c (TB10.3). The sequence of the TB10.3/4:20-28 epitope is underlined.

We then screened these peptides for their recognition by CTLs from mice infected with Mycobacterium bovis BCG or with M. tuberculosis. The effector cells of these mice specifically and efficiently lysed P815 cells pulsed with TB10.3/4:20-28 peptide or Rv3804c (Ag85A):144-152 positive-control peptide (Fig. 1B and C). The other H37Rv-derived peptides were unable to induce the lysis of target cells by such effectors. Splenocytes of controls injected with phosphate-buffered saline showed no TB10.3/4:20-28-specific CTL activity (data not shown), indicating that immunization with mycobacteria, rather than in vitro priming with TB10.3/4:20-28 peptide, induced this CTL response. The TB10.3/4:20-28 epitope is thus naturally processed and presented by MHC-I molecules in BCG- or M. tuberculosis-infected mice.

In this study, the frequency of immunogenic CTL epitopes among peptides predicted by SYFPEITHI was relatively low (1 out of 11). In a previous study using a similar bioinformatic approach on mycobacterial immunogens, this frequency was varied (4 out of 7 for H-2Kb and 1 out of 11 for H-2Dd) (16). However, recent studies show that a combination of the prediction of MHC-I ligand with information on proteasomal cleavages improves the efficiency of the identification of CD8+-T-cell epitopes (8).

Heat-killed (20 min, 86°C) BCG lost its capacity to induce a TB10.3/4:20-28-specific CTL response (Fig. 3A). This result is in agreement with the hypothesis that the most obvious way for mycobacteria to gain access to the host cell cytoplasm and its MHC-I pathway would be membrane permeabilization of the primary phagosomes inducible only by metabolically active mycobacteria (7, 14). The TB10.3/4:20-28-specific CTL activity of BCG-immunized mice was inhibited when effectors were depleted of CD8+, but not CD4+, T cells (Fig. 3B). Furthermore, TB10.3/4:20-28-loaded L fibroblasts transfected with H-2Kd, but not with H-2Dd or H-2Ld, were lysed by the CTLs of BCG-immunized mice (data not shown). Thus, immunization of mice with live BCG generates H-2Kd-restricted TB10.3/4:20-28-specific CD8+ CTLs.



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  		FIG. 3. Requirement of immunization with live BCG for induction of TB10.3/4:20-28-specific CD8+ CTLs. (A) TB10.3/4:20-28-specific CTL responses. BALB/c mice were immunized by a single s.c. injection of 107 CFU of live BCG or by two injections at a 15-day interval of 107 CFU of heat-killed BCG. Splenocytes were harvested at day 21 for CTL assay. (B) TB10.3/4:20-28-specific CTL activity of total CD4+- or CD8+-T-cell-depleted splenocytes of BCG-immunized BALB/c mice. T-subset depletion was assessed by negative selection with biotinylated anti-CD4 (GK1.5) or anti-CD8 (H35-17-2) monoclonal antibodies and streptavidin-coupled magnetic beads (Miltenyi Biotec GmbH, Bergisch Gladbach, Germany).

Using splenocytes of BCG-immunized BALB/c mice, we generated a panel of 10 CD8+-T-cell hybridomas specific for the TB10.3/4:20-28 epitope. As shown in Fig. 4A, four of these hybridomas, namely, XH3, YB8, WC7, and KC6, produce interleukin-2 (IL-2) when they are stimulated with TB10.3/4:20-28 peptide in the presence of H-2d bone marrow-derived dendritic cells. Unrelated H-2Kd-restricted Rv3804c (Ag85A):144-152 or LCMV-NP:118-126 peptides did not stimulate these hybridomas (data not shown). Assays of TB10.3/4:20-28 presentation by L fibroblasts transfected with H-2Kd, H-2Dd, or H-2Ld demonstrated that XH3 and YB8 were restricted by H-2Kd but that WC7 and KC6 were restricted by both H-2Kd and H-2Ld (data not shown). Three out of these 10 TB10.3/4:20-28-specific T-cell hybridomas efficiently recognized BCG-infected Raw 264.7 (H-2d) macrophages (Fig. 4B), indicating that the processing of mycobacteria leads to MHC-I presentation of the TB10.3/4:20-28 epitope. These hybridomas are the first-described stable CD8+-T-cell clones specific for an MHC-I-restricted mycobacterial antigen and represent powerful tools which now allow investigation of cellular and molecular mechanisms of mycobacterial-antigen presentation via the MHC-I pathway.



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  		FIG. 4. Generation of H-2Kd-restricted TB10.3/4:20-28-specific T-cell hybridomas from BCG-immunized BALB/c mice. (A) Specific IL-2 production by four TB10.3/4:20-28-specific T-cell hybridomas (XH3, YB8, WC7, and KC6) (105 cells/well) subsequent to overnight stimulation with various concentrations of TB10.3/4:20-28 peptide in the presence of syngeneic bone marrow-derived dendritic cells (105 cells/well) used as an antigen-presenting cell. (B) Specific IL-2 production (monitored by CTLL-2 bioassay) by XH3, YB8, WC7, and KC6 T-cell hybridomas in response to stimulation by Raw 264.7 macrophages incubated with 1 µg of TB10.3/4:20-28 peptide per ml or previously infected with BCG at a final concentration of 5 x 105 CFU/ml under antibiotic-free conditions for 4 days.

Based on the low quantities of ESAT-6 family proteins within in vitro mycobacterial cultures despite the substantial host immune responses to these proteins, it has been suggested that their expression may be upregulated during intracellular growth in an infected host (11). Considering (i) this hypothesis, (ii) the fact that TB10.4 is strongly recognized by peripheral blood mononuclear cells of BCG-vaccinated or tuberculosis patients (11), and (iii) our data, it might be of particular interest to investigate the potential vaccinal interest of TB10.3 or TB10.4 proteins against infection with M. tuberculosis.


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ACKNOWLEDGMENTS
 
We gratefully acknowledge Gilles Marchal for providing the BCG preparations, Richard Lo-Man for his advice on the generation of T-cell hybridomas, and Melinda Pryor for her help in bioinformatic sequence analyses of secreted or membrane mycobacterial proteins.

This work was supported by grants from the Institut Pasteur (Programme Transversal de Recherche no. 110) and INSERM E352.


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FOOTNOTES
 
* Corresponding author. Mailing address: Unité de Biologie des Régulations Immunitaires, Institut Pasteur, 25, rue du Docteur Roux, 75724 Paris Cedex 15, France. Phone: (33-1) 45.68.85.42. Fax: (33-1) 45.68.85.40. E-mail: lmajless{at}pasteur.fr. Back

Editor: S. H. E. Kaufmann


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Infection and Immunity, December 2003, p. 7173-7177, Vol. 71, No. 12
0019-9567/03/$08.00+0     DOI: 10.1128/IAI.71.12.7173-7177.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.



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