[Expression of immune cells and their roles in the involved tissues of SARS patients].

Abstract

OBJECTIVE:

To study the expression of the immune cell markers and their active antigens in the involved tissues of patients with severe acute respiratory syndrome (SARS).

METHODS:

Specimens of the lungs, spleens and lymph nodes were obtained from autopsy of 3 SARS cases to investigate the expression of the immune cells and their activities with double immunohistochemical staining (DAB and AP) by using 14 immune cell markers and their active antigens.

RESULTS:

A large quantity of proliferated macrophages could be observed in the lungs, spleens and lymph nodes of the SARS patients, some of which were positive for CD25 marker (active macrophages). In the lungs of the 3 patients, localized necrosis occurred where infiltration of CD45RO (+) T lymphocytes was observed, with only scarce Ki67 (+) T lymphocytes (active T lymphocytes) and B lymphocytes. In the lymph nodes, scattered T lymphocytes positive for Ki67 and CD45RO markers (active T lymphocytes) were seen, but the T lymphocytes subpopulations were obviously decreased, which was especially so with CD4+ and CD8+ T lymphocytes and NK cells.

CONCLUSION:

Significantly enhanced activity of the macrophages occurs in SARS as the major reactive cells, but T lymphocyte subsets are obviously decreased, indicating the important roles of the macrophages and T lymphocytes in the pathogenesis of SARS.

• Authors: Li He, Yan-qing Ding, Wei Wang, Qing-ling Zhang, Jin-hua Zhang, Jian Geng, Jun-jie Cai
• Journal: Di 1 jun yi da xue xue bao = Academic journal of the first medical college of PLA (Di Yi Jun Yi Da Xue Xue Bao) Vol. 23 Issue 8 Pg. 774-6, 780 (Aug 2003) ISSN: 1000-2588 [Print] China
• PMID: 12919894 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Ki-67 Antigen
• Leukocyte Common Antigens

Topics

• Humans
• Immunohistochemistry
• Ki-67 Antigen (analysis)
• Leukocyte Common Antigens
• Lung (immunology)
• Lymph Nodes (immunology)
• Macrophages (immunology)
• Severe Acute Respiratory Syndrome (immunology, pathology)
• Spleen (immunology)
• T-Lymphocyte Subsets (immunology)