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Clinical and Diagnostic Laboratory Immunology, January 2003, p. 140-153, Vol. 10, No. 1
1071-412X/03/$08.00+0 DOI: 10.1128/CDLI.10.1.140-153.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
California National Primate Research Center,1 Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine,2 Center for Comparative Medicine, University of California, Davis, California 95616-85423
Received 29 July 2002/ Returned for modification 23 September 2002/ Accepted 7 October 2002
Little is known regarding the timing of immune ontogeny and effector function in fetal humans and nonhuman primates. We studied the organization of lymphocyte and antigen-presenting cell populations in developing lymphoid tissues of rhesus monkey fetuses during the second and third trimesters (65 to 145 days of gestation; term = 165 days). Immunoglobulin-secreting and cytokine-secreting cells were detected at day 80. The thymus, spleen, lymph nodes, and intestinal mucosa were examined for cells expressing CD3, CD5, CD20, CD68, p55, and HLA-DR. In the spleens of 65-day-old fetuses (early second trimester), the overwhelming majority of total lymphocytes were CD5+ CD20+ B-1 cells. The remaining lymphocytes were CD3+ T cells. By day 80, splenic B and T cells were equal in number. Intraepithelial CD3+ CD5- T cells and lamina propria CD20+ CD5+ B cells were present in the intestines of 65-day-old fetuses. By day 80, numerous CD20+ CD5+ B cells were present in the jejunums and colons and early lymphocyte aggregate formation was evident. The spleens of 80- to 145-day-old fetuses contained immunoglobulin M (IgM)-secreting cells, while IgA-, IgG-, interleukin-6-, and gamma interferon-secreting cells were numerous in the spleens and colons. Thus, by the second trimester, the lymphoid tissues of the rhesus monkey fetus have a complete repertoire of properly organized antigen-presenting cells, T cells, and B cells.
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