a Department of Microbiology, Georgetown University Schools of Medicine and Dentistry, Washington, D.C. 20007
ABSTRACT
CD-1 mice immunized with sheep red blood cells (SRBC) or Escherichia coli lipopolysaccharide (LPS), developed splenic plaque-forming cells (PFC) producing low-molecular-weight antibody; these cells were detected by means of purified rabbit antisera to mouse
1,
2a, and
2b immunoglobulins. In contrast to SRBC, the primary
1 response to LPS was absent and
2a and
2b PFC were detected irregularly. Both immunogens elicited a secondary cellular response in all three subclasses without a corresponding increase in "direct" or
M PFC. An increase in serum bactericidal antibody following a second injection of LPS was not parallelled by an increase in splenic
M PFC; it might therefore involve the synthesis of
2 complement-fixing antibody.
1 Present address: Meloy Laboratories, Biological Products Division, Springfield, Va. 22151.
2 Present address: Department of Microbiology, University of Colorado Medical Center, Denver, Colo. 80220.
3 In partial fulfillment of the requirements for the Doctor of Philosophy Degree, Georgetown University.
| J. Bacteriol. | J. Virol. | Eukaryot. Cell |
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| Microbiol. Mol. Biol. Rev. | Clin. Vaccine Immunol. | All ASM Journals |
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