1977
DOI: 10.1159/000240937
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Thymus-Dependent Lymphocytes and Delayed Hypersensitivity in Low Birth Weight Infants

Abstract: The proportion of thymus-dependent (T) lymphocytes in the blood and the ability to mount cutaneous delayed hypersensitivity to a battery of antigens were evaluated in 50 low birth weight (LBW) infants when they were 3 months to 5 years old. There was a significant reduction in the number of T lymphocytes. Delayed hypersensitivity was impaired. The abnormalities were more pronounced in those with persistent growth retardation. It is suggested that continued postnatal depression of cell-mediated immunity in LBW … Show more

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Cited by 40 publications
(14 citation statements)
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“…More interesting are differences in the phenotype, cytokine profiles and function of lymphocytes of nephrotic patients during relapse in remission [48][49][50][51]. In immunological studies of SGA cohorts, a reduced number of T cells, a higher number of CD8-positive cells and delayed hypersensitivity reaction were detectable [52,53]. Knowledge of the immunological consequences of IUGR is limited at the moment.…”
Section: Discussionmentioning
confidence: 99%
“…More interesting are differences in the phenotype, cytokine profiles and function of lymphocytes of nephrotic patients during relapse in remission [48][49][50][51]. In immunological studies of SGA cohorts, a reduced number of T cells, a higher number of CD8-positive cells and delayed hypersensitivity reaction were detectable [52,53]. Knowledge of the immunological consequences of IUGR is limited at the moment.…”
Section: Discussionmentioning
confidence: 99%
“…In addition, malnourished children have a reduced saliva secretion rate and buffering capacity, lower calcium and protein secretion in stimulated saliva, and impaired immunological and agglutinating defence factors in unstimulated saliva [Johansson et al, 1992[Johansson et al, , 1994. Finally, low birth weight has been associated with lower levels of IgG, IgA and IgM [Ballow et al, 1986], lower antibody titers, lower numbers of circulating T cells and complement factors [Chandra et al, 1977;Chandra and Matsumura, 1980;Chandra, 1988], which partly explains the higher incidence of infections in low birth weight infants through the first 10 months of life. By contrast, normal birth weight infants achieve normal immune function by 3 months [Chandra, 1981[Chandra, , 1986.…”
Section: Discussionmentioning
confidence: 99%
“…Increased growth in utero may therefore lead to an increased risk of later immune mediated destruction of the pancreatic β cells. Low birth weight has been associated with impaired cellular immune competence up to 5 years of age29 and with increased mortality from infectious diseases in the age group 1-15 years. 17 30 Perhaps an impaired cellular immune response makes children less prone to immune mediated destruction of the β cells?…”
Section: Discussionmentioning
confidence: 99%