Hepatitis B virus-reactive human T-lymphocyte clones: Antigen specificity and helper function or antibody synthesis
- E. Celis,
- P. C. Kung,
- T. W. Chang
- Centocor, Inc.
Sustainable Development Goals
- SDG 3 Good Health and Well
Abstract
To study immunity to hepatitis B surface antigen (HBsAg) at the cellular level, lymphocytes were obtained from the peripheral blood of hepatitis B vaccine recipients and were examined for various immune responses to HBsAg in vitro. The peripheral blood mononuclear cells (PBM) from most of the vaccinees did not proliferate to a great extent to HBsAg in vitro. However, HBsAg-reactive lymphocyte lines and clones were obtained from some of these individuals if the PBM were stimulated in vitro with HBsAg and were maintained in the presence of T cells growth supplement. Most of the HBsAg-reactive T cell clones obtained were found to be antigen-specific and some of them provided help in the production of anti-HBsAg antibodies by a cell population enriched for HBsAg-binding cells. These results indicate that HBsAg-specific T and B cells exist in the circulation of hepatitis B vaccine recipients, although they are at limiting concentrations for the in vitro cell proliferation and antibody production assays.
Publication Information
Output type
Original language
English (US)Pages from-to (Number of pages)
Pages 1511-1516 (6 pages)Journal (Volume, Issue Number)
Journal of Immunology (Volume 132, Issue 3)Publication milestones
- Published - 1984
Publication status
ISSN
0022-1767Publication IDs
- Scopus: 0021346972
- PubMed: 6198394
