4.6 Article

Lack of Original Antigenic Sin in Recall CD8(+) T Cell Responses

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JOURNAL OF IMMUNOLOGY
卷 184, 期 11, 页码 6320-6326

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AMER ASSOC IMMUNOLOGISTS
DOI: 10.4049/jimmunol.1000149

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资金

  1. Howard Hughes Medical Institute
  2. German Research Foundation (Deutsche Forschungsgemeinschaft)
  3. National Institutes of Health [AI19335, U54 AI081680]
  4. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [R01AI076457, R37AI019335, U54AI081680, P01AI056172, R01AI019335] Funding Source: NIH RePORTER

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In the real world, mice and men are not immunologically naive, having been exposed to numerous antigenic challenges. Prior infections sometimes negatively impact the response to a subsequent infection. This can occur in serial infections with pathogens sharing cross-reactive Ags. At the T cell level it has been proposed that preformed memory T cells, which cross-react with low avidity to epitopes presented in subsequent infections, dampen the response of high-avidity T cells. We investigated this with a series of related MHC class-I restricted Ags expressed by bacterial and viral pathogens. In all cases, we find that high-avidity CD8(+) T cell precursors, either naive or memory, massively expand in secondary cross-reactive infections to dominate the response over low-avidity memory T cells. This holds true even when >10% of the CD8(+) T cell compartment consists of memory T cells that cross-react weakly with the rechallenge ligand. Occasionally, memory cells generated by low-avidity stimulation in a primary infection recognize a cross-reactive epitope with high avidity and contribute positively to the response to a second infection. Taken together, our data show that the phenomenon of original antigenic sin does not occur in all heterologous infections. The Journal of Immunology, 2010, 184: 6320-6326.

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