The life history of isotype-switched B cells is unclear, in part, because of an inability to detect rare antigen-specific B cells at early times during the immune response. To address this issue, a small population of B cells carrying targeted antibody transgenes capable of class switching was monitored in immunized mice. After contacting helper T cells, the first switched B cells appeared in follicles rather than in the red pulp, as was expected. Later, some of the switched B cells transiently occupied the red pulp and marginal zone, whereas others persisted in germinal centers (GCs). Antigen-experienced IgM B cells were rarely found in GCs, indicating that these cells switched rapidly after entering GCs or did not persist in this environment.
Visualization of the Genesis and Fate of Isotype-switched B Cells during a Primary Immune Response
The present address of Valerie Kouskoff is Mount Sinai School of Medicine, Icahn Institute for Gene Therapy and Molecular Medicine, New York, NY 10029.
The present address of H. Lucy Tang is Tularik, 2 Corporate Dr., South San Francisco, CA 94080.
Abbreviations used in this paper: BCR, B cell receptor; CFSE, carboxyfluorescein diacetate succinimidyl ester; DEL, duck egg lysozyme; GC, germinal center; HEL, hen egg lysozyme; HRP, horseradish peroxidase; KIH, knockin homozygous; OVA-mim, OVA-mimotope–expressing bacteriophage; PALS, periarteriolar lymphoid sheaths.
Kathryn A. Pape, Valerie Kouskoff, David Nemazee, H. Lucy Tang, Jason G. Cyster, Lina E. Tze, Keli L. Hippen, Timothy W. Behrens, Marc K. Jenkins; Visualization of the Genesis and Fate of Isotype-switched B Cells during a Primary Immune Response . J Exp Med 16 June 2003; 197 (12): 1677–1687. doi: https://doi.org/10.1084/jem.20012065
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