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PMID: 291990 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Cell cytotoxicity due to specific influenza antibody production in vitro after recent influenza antigen stimulation.

Greenberg SB, Six HR, Drake S, Couch RB

Abstract

Peripheral blood leukocytes, obtained from volunteers after vaccination or natural illness with influenza, were assayed for cytotoxicity against influenza virus-infected cells. Approximately 7 days after vaccination or the onset of respiratory illness, peak cytotoxicity was demonstrated in a chromium-release assay. Secretion of specific antibody against hemagglutinin from the leukocytes during in vitro incubation was demonstrated in quantities that would mediate the cell cytotoxicity observed. Antibody secretion was inhibited by exposure to cycloheximide but not by exposure to trypsin. The secretion of antibody against hemagglutinin from peripheral blood leukocytes occurred only at the time of maximal cytotoxicity. We thus demonstrate secretion of specific antibody in vitro after recent viral antigen stimulation. Moreover, this antibody is capable of conveying cytotoxic capacity to peripheral blood leukocytes that may be important in the recovery process from acute viral infection.

MeSH Terms
Antibodies, Viral Antibody Formation Antigens, Viral Cycloheximide/pharmacology Cytotoxicity, Immunologic Hemagglutinins, Viral Humans Immunity, Cellular Immunologic Memory Influenza A virus/immunology Lymphocytes/immunology Trypsin/metabolism Vaccination Viral Vaccines
Chemicals
Antibodies, Viral Antigens, Viral Hemagglutinins, Viral Viral Vaccines Cycloheximide Trypsin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Greenberg S B
Six H R
Drake S
Couch R B
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25 references, click to expand
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Article Info
Journal
Proceedings of the National Academy of Sciences of the United States of America
Abbr.
Proc Natl Acad Sci U S A
ISSN
0027-8424
Published
1979-09-00
Pages
4622-6
Language
English
Region
United States
NLM ID
7505876
PMCID
PMC411631
Subset
IM
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