PMID- 11709514 OWN - NLM STAT- MEDLINE DCOM- 20011228 LR - 20220316 IS - 0017-5749 (Print) IS - 1458-3288 (Electronic) IS - 0017-5749 (Linking) VI - 49 IP - 6 DP - 2001 Dec TI - Interleukin 16 expression and phenotype of interleukin 16 producing cells in Crohn's disease. PG - 795-803 AB - BACKGROUND: The mechanisms involved in the initiation and maintenance of Crohn's disease are poorly understood. Previous studies have demonstrated an increased number of infiltrating CD4+ T cells within the inflammatory affected bowel wall in Crohn's disease. Novel therapy approaches using anti-CD4 antibodies are thought to be effective in Crohn's disease. AIMS: Interleukin 16 (IL-16) has been characterised as a chemokine with selective chemoattraction for CD4+ inflammatory T cells. In this study, cellular expression of IL-16 in Crohn's disease and ulcerative colitis was investigated. METHODS: Expression of IL-16 was analysed in tissue samples of Crohn's disease, ulcerative colitis, and normal controls by applying reverse transcription-polymerase chain reaction, non-radioactive in situ hybridisation, and immunohistochemistry. Double staining methods were used to characterise cells expressing IL-16. The amount of infiltrating CD4+ cells was determined by immunohistochemistry and correlated with the corresponding IL-16+ cell number by step sections. RESULTS: An increased number of IL-16+ cells in Crohn's disease in comparison with ulcerative colitis and control probes was demonstrated. IL-16 was expressed by CD4 and CD8 positive T cells. In addition, in active Crohn's disease there was a substantial number of IL-16 positive mast cells. The increased number of CD4+ lymphocytes correlated positively with the increased number of IL-16 positive cells in Crohn's disease. CONCLUSION: Our results demonstrate that increased expression of IL-16 in T cells and mast cells in active Crohn's disease is associated with increased numbers of CD4+ lymphocytes. Local expression of IL-16 seems to play a significant role in the initiation and persistence of the inflammatory process in Crohn's disease, presumably by IL-16 mediated recruitment of CD4+ cells, mostly lymphocytes, into the bowel wall. FAU - Middel, P AU - Middel P AD - Department of Pathology, Georg-August University of Gottingen, Germany. pmiddel@med.uni-goettingen.de FAU - Reich, K AU - Reich K FAU - Polzien, F AU - Polzien F FAU - Blaschke, V AU - Blaschke V FAU - Hemmerlein, B AU - Hemmerlein B FAU - Herms, J AU - Herms J FAU - Korabiowska, M AU - Korabiowska M FAU - Radzun, H J AU - Radzun HJ LA - eng PT - Comparative Study PT - Journal Article PL - England TA - Gut JT - Gut JID - 2985108R RN - 0 (Interleukin-16) SB - IM CIN - Gut. 2001 Dec;49(6):747-8. PMID: 11709502 MH - Adolescent MH - Adult MH - CD4 Lymphocyte Count MH - CD4-Positive T-Lymphocytes/immunology MH - CD8-Positive T-Lymphocytes/immunology MH - Chemotaxis, Leukocyte MH - Colitis, Ulcerative/immunology MH - Colon/immunology MH - Crohn Disease/*immunology MH - Female MH - Humans MH - Immunohistochemistry/methods MH - In Situ Hybridization/methods MH - Interleukin-16/*analysis MH - Male MH - Mast Cells/immunology MH - Middle Aged MH - Phenotype MH - Reverse Transcriptase Polymerase Chain Reaction MH - T-Lymphocytes/*immunology PMC - PMC1728558 EDAT- 2001/11/16 10:00 MHDA- 2002/01/05 10:01 PMCR- 2004/12/01 CRDT- 2001/11/16 10:00 PHST- 2001/11/16 10:00 [pubmed] PHST- 2002/01/05 10:01 [medline] PHST- 2001/11/16 10:00 [entrez] PHST- 2004/12/01 00:00 [pmc-release] AID - 10.1136/gut.49.6.795 [doi] PST - ppublish SO - Gut. 2001 Dec;49(6):795-803. doi: 10.1136/gut.49.6.795.