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Differential kinetics of antigen-specific CD4+ and CD8+ T cell responses in the regression of retrovirus-induced sarcomas.

Koen Schepers ,
Mireille Toebes ,
Gitte Sotthewes ,
Florry A Vyth-Dreese ,
Trees A M Dellemijn ,
Cornelis J M Melief ,
Ferry Ossendorp ,
Ton N M Schumacher

Abstract

Despite the accepted role for CD4+ T cells in immune control, little is known about the development of Ag-specific CD4+ T cell immunity upon primary infection. Here we use MHC class II tetramer technology to directly visualize the Ag-specific CD4+ T cell response upon infection of mice with Moloney murine sarcoma and leukemia virus complex (MoMSV). Significant numbers of Ag-specific CD4+ T cells are detected both in lymphoid organs and in retrovirus-induced lesions early during infection, and they express the 1B11-reactive activation-induced isoform of CD43 that was recently shown to define effector CD8+ T cell populations. Comparison of the kinetics of the MoMSV-specific CD4+ and CD8+ T cell responses reveals a pronounced shift toward CD8+ T cell immunity at the site of MoMSV infection during progression of the immune response. Consistent with an important early role of Ag-specific CD4+ T cell immunity during MoMSV infection, CD4+ T cells contribute to the generation of virus-specific CD8+ T cell immunity within the lymphoid organs and are required to promote an inflammatory environment within the virus-infected tissue.

More about this publication

Journal of immunology (Baltimore, Md. : 1950)

Volume 169
Issue nr. 6
Pages 3191-9
Publication date 15-09-2002

Full text links

Publisher website (DOI) 10.4049/jimmunol.169.6.3191
Europe PubMed Central 12218137
Pubmed 12218137

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