Tumor Immune Systems in Esophageal Cancer with Special Reference to Heat-shock Protein 70 and Humoral Immunity
The objective of this study was to clarify the participation of heat-shock protein 70 (HSP70) and the humoral immune system in antitumor immunity in esophageal cancer. Patients and Methods: Immunohistochemical staining for HSP 70, and CD4 + T-, CD8 + T-, B- and plasma cells was performed on surgical...
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Published in: | Anticancer research Vol. 29; no. 5; pp. 1595 - 1606 |
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Main Authors: | , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
Attiki
International Institute of Anticancer Research
01-05-2009
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Online Access: | Get full text |
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Summary: | The objective of this study was to clarify the participation of heat-shock protein 70 (HSP70) and the humoral immune system
in antitumor immunity in esophageal cancer. Patients and Methods: Immunohistochemical staining for HSP 70, and CD4 + T-, CD8 + T-, B- and plasma cells was performed on surgical specimens obtained from 125 patients with esophageal cancer. An enzyme-linked
immunosorbent assay (ELISA) was then performed to measure serum anti-HSP70 antibodies in the azygos vein. Results: The expression
of HSP 70 correlated inversely with depth of invasion (p<0.0001), pathological stage (p<0.0001) and blood vessel invasion
(p<0.001), and there was a positive correlation between HSP70 and CD4 + T-, CD8 + T-, B- and plasma cells. Of these, the B- and plasma cells had the strongest correlation to HSP70 expression. Serum anti-HSP70
antibody levels in the azygos vein correlated with HSP70 expression, and B and plasma cell infiltration. Patients positive
for HSP70, and B- and plasma cell infiltration had good prognosis compared to other cases. According to multivariate analyses,
simultaneous occurrence of HSP70 expression, and B- and plasma cell infiltration is a stronger prognostic factor than simultaneous
occurrence of HSP70 expression, and CD4 + T- and CD8 + T-cell infiltration. Conclusion: It is suggested that the HSP70-humoral immune cell system might play an important role in
antitumor effects in patients with esophageal cancer. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0250-7005 1791-7530 |