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Usage Information

Cell-Mediated Immunity during Natural Measles Infection
H. C. Whittle, J. Dossetor, A. Oduloju, A. D. M. Bryceson, B. M. Greenwood
H. C. Whittle, J. Dossetor, A. Oduloju, A. D. M. Bryceson, B. M. Greenwood
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Research Article

Cell-Mediated Immunity during Natural Measles Infection

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Abstract

Natural measles causes prolonged depression of cell-mediated immunity yet little is known as to how the infection influences lymphocyte function. Therefore, we studied the properties and function of lymphocytes during and after measles. The number and proportion of circulating thymus-derived lymphocytes was low during the acute stage of measles, and at this time 37% of these cells showed positive immunofluorescent staining for measles virus after stimulation with phytohemagglutinin. 7% of B cells were shown to contain virus but their numbers did not alter during the infection. Acute-phase lymphocytes, when stimulated, yielded infective virus and half were killed on incubation with autologous serum and complement. In acute measles the increase in [3H]-thymidine uptake of lymphocytes when stimulated with an optimal dose of PHA was normal in media with 10% fetal calf serum and low in media containing 10% autologous serum: the mean values were 56.8±34.1 and 23.7±25.9 cpm × 103 per 106 lymphocytes, respectively. Stimulation of acute-phase lymphocytes by Candida antigen was also low in media containing autologous serum averaging 1.2 × 103 cpm per 106 lymphocytes. On recovery 4-6 wk later this rose significantly to 18.9±19.8. The mean migration index of leukocytes to heat-killed candida cells in acute measles was 0.84±SD 0.08, and this fell significantly to 0.75±SD 0.08 4 wk later. Thus, depletion of T cells, an inhibitor of lymphocyte proliferation in the serum and a possible defect in antigen processing, interacts to depress cell-mediated immunity in measles.

Authors

H. C. Whittle, J. Dossetor, A. Oduloju, A. D. M. Bryceson, B. M. Greenwood

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Usage data is cumulative from November 2025 through November 2026.

Usage JCI PMC
Text version 326 19
PDF 150 11
Scanned page 410 0
Citation downloads 180 0
Totals 1,066 30
Total Views 1,096
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Usage information is collected from two different sources: this site (JCI) and Pubmed Central (PMC). JCI information (compiled daily) shows human readership based on methods we employ to screen out robotic usage. PMC information (aggregated monthly) is also similarly screened of robotic usage.

Various methods are used to distinguish robotic usage. For example, Google automatically scans articles to add to its search index and identifies itself as robotic; other services might not clearly identify themselves as robotic, or they are new or unknown as robotic. Because this activity can be misinterpreted as human readership, data may be re-processed periodically to reflect an improved understanding of robotic activity. Because of these factors, readers should consider usage information illustrative but subject to change.

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Copyright © 2026 American Society for Clinical Investigation
ISSN: 0021-9738 (print), 1558-8238 (online)

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