PMID- 10981527 OWN - NLM STAT- MEDLINE DCOM- 20010126 LR - 20191104 IS - 0905-6157 (Print) IS - 0905-6157 (Linking) VI - 11 IP - 3 DP - 2000 Aug TI - Expression of and responses to CD2 and CD3 in 18-month-old children with and without atopic dermatitis. PG - 175-82 AB - We hypothesize that atopy is associated with a reduced T-cell function early in life and an imbalance in cytokine production. The purpose of this study was to investigate the expression of and responses to CD2 and CD3 in children who did or did not develop atopic dermatitis early in life. The expression of CD2 and CD3 was analyzed by flow cytometry, and proliferation of CD2 and CD3 was studied by 3H-thymidine incorporation in phytohaemagglutinin (PHA)- and anti-CD3-stimulated peripheral blood mononuclear cells (PBMC) of 18-month-old children, 25 with and 29 without atopic dermatitis. Exogenous interleukin (IL)-2 was added to compensate for possible functional differences in accessory cells. Anti-CD3-induced secretion of IL-4, IL-5, IL-6, IL-10, IL-13, and interferon-gamma (IFN-gamma) was analyzed by enzyme-linked immunosorbent assay (ELISA). Atopy was associated with a low proportion of CD2+ lymphocytes. Responsiveness to PHA, which activates lymphocytes partly via the sheep erythrocyte receptor, CD2, was reduced in the allergic children. The anti-CD3-induced proliferation declined more rapidly with antibody dilution in the allergic than in the non-allergic children. Atopic dermatitis was associated with high levels of anti-CD3-stimulated IL-5 secretion. The IL-4/IL-10 and IL-4/ITFN-gamma ratios were higher in children with elevated total immunoglobulin E (IgE) levels. Skin prick test-negative children with eczema produced higher levels of IL-10 than skin prick test-positive children. In conclusion, atopic children have a reduced T-cell function. Atopic dermatitis is associated with increased IL-5 production, while high total IgE levels are associated with high IL-4/IFN-gamma and IL-4/IL-10 ratios. FAU - Jenmalm, M C AU - Jenmalm MC AD - Department of Health and Environment, Clinical Research Center, Faculty of Health Sciences, Linkoping University, Sweden. Maria.Jenmalm@kfc.liu.se FAU - Aniansson-Zdolsek, H AU - Aniansson-Zdolsek H FAU - Holt, P G AU - Holt PG FAU - Bjorksten, B AU - Bjorksten B LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - England TA - Pediatr Allergy Immunol JT - Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology JID - 9106718 RN - 0 (CD2 Antigens) RN - 0 (CD3 Complex) RN - 0 (Interleukin-13) RN - 0 (Interleukin-5) RN - 0 (Interleukin-6) RN - 130068-27-8 (Interleukin-10) RN - 207137-56-2 (Interleukin-4) RN - 82115-62-6 (Interferon-gamma) SB - IM MH - CD2 Antigens/*biosynthesis/immunology MH - CD3 Complex/*biosynthesis/immunology MH - Dermatitis, Atopic/*immunology MH - Female MH - Humans MH - Infant MH - Interferon-gamma/biosynthesis MH - Interleukin-10/biosynthesis MH - Interleukin-13/biosynthesis MH - Interleukin-4/biosynthesis MH - Interleukin-5/biosynthesis MH - Interleukin-6/biosynthesis MH - Male MH - Surveys and Questionnaires MH - T-Lymphocytes/*immunology EDAT- 2000/09/12 11:00 MHDA- 2001/02/28 10:01 CRDT- 2000/09/12 11:00 PHST- 2000/09/12 11:00 [pubmed] PHST- 2001/02/28 10:01 [medline] PHST- 2000/09/12 11:00 [entrez] AID - 10.1034/j.1399-3038.2000.00083.x [doi] PST - ppublish SO - Pediatr Allergy Immunol. 2000 Aug;11(3):175-82. doi: 10.1034/j.1399-3038.2000.00083.x.