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Clinical and Diagnostic Laboratory Immunology, 05 1997, 375-379, Vol 4, No. 3
S Baqar, AA Nour El Din, DA Scott, AL Bourgeois, AS Mourad, MT Kleinosky, MJ Oplinger and JR Murphy
A sensitive, and at times the most sensitive, measurement of human vaccine
immunogenicity is enumeration of antibody-secreting cells (ASC) in
peripheral blood. However, this assay, which is inherently capable of
measurement of the absolute number of antigen-specific ASC, is not
standardized. Thus, quantitative comparison of results between laboratories
is not currently possible. To address this issue, isotype- specific ASC
were enumerated from paired fresh and cryopreserved mononuclear cell (MNC)
preparations from healthy adult volunteers resident in either the United
States (US group) or Egypt (EG group). Analysis of fresh cells from US
volunteers revealed mean numbers of ASC per 10(6) MNC of 617, 7,738, and
868 for immunoglobulin M (IgM), IgG, and IgA, respectively, whereas EG
volunteers had 2,086, 7,580, and 1,677 ASC/10(6) MNC for the respective
isotypes. Cryopreservation resulted in a slight reduction in group mean
IgM, IgG, and IgA ASC (maximum reduction in group mean, 14%), but in no
instance were results obtained with cryopreserved cells significantly lower
than those obtained with fresh cells. To determine if cryopreservation
affected the number of bacterial antigen-specific ASC detected, cells from
a group of US adult volunteers who received a single oral dose of a mutated
Escherichia coli heat-labile enterotoxin (LT(R192G)) were tested. There was
no significant difference (P > 0.05) in the number of antigen-specific
IgA or IgG ASC detected between fresh and cryopreserved MNC. The results
support the views that ASC assays can be standardized to yield quantitative
results and that the methodology can be changed to make the test more
practical.
Copyright © 1997 by the American Society for Microbiology. All rights reserved.
Standardization of measurement of immunoglobulin-secreting cells in human peripheral circulation
Department of Infectious Diseases, Naval Medical Research Institute, Bethesda, Maryland, USA.
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