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In situ studies of the primary immune response to (4-hydroxy-3-nitrophenyl)acetyl. I. The architecture and dynamics of responding cell populations.
Abstract
After primary immunization with an immunogenic conjugate of (4-hydroxy-3-nitrophenyl)acetyl,
two anatomically and phenotypically distinct populations of antibody-forming cells
arise in the spleen. As early as 2 d after immunization, foci of antigen-binding B
cells are observed along the periphery of the periarteriolar lymphoid sheaths. These
foci expand, occupying as much as 1% of the splenic volume by day 8 of the response.
Later, foci grow smaller and are virtually absent from the spleen by day 14. A second
responding population, germinal center B cells, appear on day 8-10 and persist at
least until day 16 post-immunization. Individual foci and germinal centers represent
discrete pauciclonal populations that apparently undergo somatic evolution in the
course of the primary response. We suggest that foci may represent regions of predominantly
interclonal competition for antigen among unmutated B cells, while germinal centers
are sites of intraclonal clonal competition between mutated sister lymphocytes.
Type
Journal articleSubject
AnimalsAntibodies
Antibody Formation
Antigens
B-Lymphocytes
Base Sequence
Cell Division
DNA
Immunoglobulin Isotypes
Immunoglobulin Switch Region
Immunoglobulin Variable Region
Immunoglobulin lambda-Chains
Mice
Mice, Inbred BALB C
Mice, Inbred C57BL
Molecular Sequence Data
Nitrophenols
Nucleic Acid Hybridization
Phenotype
Phenylacetates
Spleen
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https://hdl.handle.net/10161/11490Collections
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Show full item recordScholars@Duke
Garnett H. Kelsoe
James B. Duke Distinguished Professor of Immunology
1. Lymphocyte development and antigen-driven diversification of immunoglobulin and
T cell antigen receptor genes. 2. The germinal center reaction and mechanisms for
clonal selection and self - tolerance. The origins of autoimmunity. 3. Interaction
of innate- and adaptive immunity and the role of inflammation in lymphoid organogenesis.
4. The role of secondary V(D)J gene rearrangment in lymphocyte development and malignancies.
5. Mathematical modeling of immune responses,

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