scholarly journals High frequency of cross-reactive cytotoxic T lymphocytes elicited during the virus-induced polyclonal cytotoxic T lymphocyte response.

1993 ◽  
Vol 177 (2) ◽  
pp. 317-327 ◽  
Author(s):  
S R Nahill ◽  
R M Welsh

Polyclonal stimulation of CD8+ cytotoxic T lymphocytes (CTL) occurs during infection with many viruses including those not known to transform CTL or encode superantigens. This polyclonal CTL response includes the generation of high levels of allospecific CTL directed against many class I haplotypes. In this report we investigated whether the allospecific CTL generated during an acute lymphocytic choriomeningitis virus (LCMV) infection of C57BL/6 mice were stimulated specifically by antigen recognition or nonspecifically by polyclonal mechanisms possibly involving lymphokines or superantigens. An examination of the ability of different strains of mice to induce high levels of CTL specific for a given alloantigen showed that most, but not all, strains generated high levels of allospecific CTL, and that their abilities to generate them mapped genetically to the major histocompatibility complex locus, exclusive of the class II region. This indicated that the virus-induced allospecific CTL generation was independent of the class II allotype, and mice depleted of CD4+ cells generated allospecific CTL, indicating independence of class II-CD4+ cell interactions and resulting CD4+ cell-secreted lymphokines. FACS staining with a variety of V beta-binding antibodies did not show a superantigen-like depletion or enrichment of any tested V beta + subset during infection. Several experiments provided evidence in support of direct stimulation of CD8+ cells via the T cell receptor: (a) both virus- and allo-specific killing were enriched within a given V beta subpopulation; (b) relative CTL precursor frequencies against different class I alloantigens changed during the course of virus infection; (c) the relative levels of virus-induced, allospecific CTL-mediated lysis at day 8 after infection did not parallel the CTL precursor frequencies before infection; and (d) limiting dilution analyses of day 8 LCMV-infected spleen cells stimulated by virus-infected syngeneic peritoneal exudate cells (PEC) revealed not only the expected virus-specific CTL clones, but also a high frequency of clones that were cross-reactive with allogeneic and virus-infected syngeneic targets. In addition to the virus cross-reactive allospecific CTL clones, virus-infected PEC also stimulated the generation of some allospecific clones that did not lyse virus-infected fibroblasts. Surprisingly, LCMV-infected PEC were much more efficient at stimulating allospecific CTL clones from day 8 LCMV-infected splenocytes than were allogeneic stimulators. These results indicate that at least part of the polyclonal allospecific CTL response elicited by acute virus infection is a consequence of the selective expansion of many clones of allospecific CTL which cross-react with virus-infected cells.(ABSTRACT TRUNCATED AT 400 WORDS)

1987 ◽  
Vol 165 (6) ◽  
pp. 1508-1523 ◽  
Author(s):  
J Bastin ◽  
J Rothbard ◽  
J Davey ◽  
I Jones ◽  
A Townsend

The conserved epitopes of influenza nucleoprotein (NP) recognized by class I MHC-restricted CTL from CBA (H-2k) and C57BL/10 (H-2b) mice have been defined in vitro with synthetic peptides 50-63 and 365-379, respectively. Two Db-restricted clones were described that recognize different epitopes on peptide 365-379. Finally, the recognition of complete NP was shown to be approximately 200-fold less efficient than peptide in the cytotoxicity assay. These phenomena are closely related to results with class II-restricted T cells and they strengthen the hypothesis that influenza proteins are degraded in the infected cell before recognition by class I-restricted CTL.


Blood ◽  
2004 ◽  
Vol 104 (11) ◽  
pp. 3848-3848
Author(s):  
Hironari Niiya ◽  
Jin Lei ◽  
Ikuya Sakai ◽  
Taichi Azuma ◽  
Naoyuki Uchida ◽  
...  

Abstract Background: Cytotoxic T lymphocytes (CTLs) play a crucial role in resistance against viral infections and cancer development. The conventional CTLs are MHC class I-restricted CD8+ T lymphocytes; however, MHC class II-restricted CD4+ CTLs directed against alloantigen and various kinds of virus and cancer are also present. We have reported recently that human CD4+ as well as CD8+ CTLs exert antigen-specific cytotoxicity through perforin-dependent cytolytic pathway (Blood95:2352–2355,2000; J. Immunol.170:2205–2213,2003). Although antigen-specific CD4+ CTLs can be generated generally in the in vitro culture systems, their significance in resistance against infections and malignancies in vivo is still obscure. Because perforin is the important cytolytic mediator of human CD4+ as well as CD8+ CTLs, understanding the regulatory mechanisms of perforin expression in CD4+ and CD8+ CTLs seems an important issue. Based on this background, we addressed the question of whether perforin expression is differentially regulated in CD4+ and CD8+ CTLs. Methods: Herpes simplex virus (HSV)-specific and HLA class II-restriced CD4+ CTL clones and Epstein-Barr virus (EBV)-specific and HLA class I-restricted CD8+ CTL clones were established from healthy individuals. CTL clones were used for experiments after 3 to 5 days of viral antigen stimulation, when they were in activated phase and after 12 to 15 days, when they were in resting phase. The cytotoxic activity of activated and resting CTL clones was measured by standard 51Cr release assays. Perforin mRNA expression levels in CTLs were determined by quantitative RT-PCR. Expression of surface molecules on CTL clones was examined by flow cytometry. To compare the binding activity of STAT to the perforin promoter in CD4+ and CD8+ CTLs, electrophoretic mobility shift assay (EMSA) was performed using a STAT-binding probe. Results: The degrees of antigen-specific cytotoxicity mediated by CD8+ CTLs were not significantly different in activated and resting phase; however, cytotoxicity of CD4+ CTLs in resting phase appeared to be significantly lower than that in activated phase. Similarly, perforin mRNA expression levels in activated and resting CD8+ CTLs were not significantly different, but activated CD4+ CTLs appeared to express abundant perforin compared to resting CD4+ CTLs. Expression levels of all surface functional molecules except CD25 are not significantly different between activated and resting CD4+ and CD8+ CTL clones. Interestingly, binding activity of STAT5 to promoter for perforin gene appeared to increase in activated CD4+ CTLs compared to that in resting CD4+ CTLs. In contrast, no significant difference of STAT5 binding activity to promoter for perforin gene was detected between activated and resting CD8+ CTLs. Conclusion: The present study revealed the different control of perforin expression in CD4+ and CD8+ CTLs; that is, perfron is expressed constitutively in CD8+ CTLs but perforin expression in CD4+ CTLs is cell-activation-dependent.


1993 ◽  
Vol 67 (4) ◽  
pp. 2276-2284 ◽  
Author(s):  
R S van Binnendijk ◽  
J P Versteeg-van Oosten ◽  
M C Poelen ◽  
H F Brugghe ◽  
P Hoogerhout ◽  
...  

1986 ◽  
Vol 163 (4) ◽  
pp. 972-980 ◽  
Author(s):  
N Shinohara ◽  
J A Bluestone ◽  
D H Sachs

Cloned CTLs QM3 and QM7 isolated from a bulk CTL line B10.QBR anti-B10.MBR recognized a combination of the H-2Kb molecule and an I-Ak subregion gene product. Such a combinatorial specificity was revealed by complementation of the target antigen in F1 animals between two negative parental strains carrying H-2Kb and I-Ak, respectively. We confirmed the involvement of the H-2Kb molecule by blocking killing with anti-Kb mAb and failure of certain mutant H-2Kb genes to complement with I-Ak to generate the determinant in F1 animals. Although the nature of the I-Ak subregion gene product is not definitive, there was a correlation between the expression of Ia antigens on the cell surface and susceptibility of the cells to lysis by these CTLs, suggesting that it is the classical I-Ak class II antigen.


1988 ◽  
Vol 62 (10) ◽  
pp. 3756-3763 ◽  
Author(s):  
K Maier ◽  
P Gabriel ◽  
E Koscielniak ◽  
Y D Stierhof ◽  
K H Wiedmann ◽  
...  

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