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PMID: 16111767 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Review

Current concepts of tumor-infiltrating lymphocytes in human malignancies.

Journal of reproductive immunology ·Vol. 67 ·No. 1-2 ·2005-10-00 ·Pages 35-50

Chiou SH, Sheu BC, Chang WC, Huang SC, Hong-Nerng H

Abstract

Tumor-infiltrating lymphocytes (TILs) develop as manifestations of the recognition and defense against malignant cells by the host immune system. TILs were literally defined as "tumor-infiltrating lymphocytes", which a posteriori locate within the tumor tissues. Although such cells can be found, they fail to control the growth of tumor. Many have proposed diverse mechanisms for dysfunction of TILs with regard to the roles of immunosurveillance against cancer. However, only a few cancer types, e.g. melanoma, have seen the benefits brought by activating these cells for immunotherapy. Functional defects of TILs have been linked to abnormalities of signaling molecules; however, there is conflicting data. The death of TILs was attributed to expression of cancer-derived FasL, PD-1 and RCAS1, and cancer-induced activation-induced cell death (AICD). Confirmed by studies using TILs and animal models, the compromise of tumor-specific immune responses was thought to result from not only mechanisms of clonal anergy but also exhaustion and/or deletion. Furthermore, functional cytotoxic CD8(+) TILs might be rendered incompetent by cancer-induced up-regulation of inhibitory NK receptors or proximal signaling abnormalities. Additionally, immune privilege was partly attributed to recruitment of regulatory T cells to the tumor sites. The failure of IL-2 signaling, which stands at the center of T cell functionalities, had been linked to the enzymatic activity of cancer-derived matrix metalloproteinases (MMPs). Finally, the exploitation of IDO expression, an important enzyme in pregnancy-related immunosuppression, by cancer cells might play a role in tumor immunity. The disparity of cancer types, origin, developmental stages and individual genetic backgrounds likely account for differences, or even contradictions, which might be the reason why immunotherapy works only on a few cancer types. Delineating the mechanisms behind functional defects of TILs can help not only boost chances of the development of a successful cure but understand the not fully identified roles played by immune system in the face of malignancies.

MeSH Terms
Female Humans Immunologic Surveillance Immunotherapy Lymphocyte Activation/immunology Lymphocyte Subsets/immunology Lymphocytes, Tumor-Infiltrating/immunology Melanoma/immunology,therapy Neoplasm Proteins/immunology Pregnancy Signal Transduction/immunology
Chemicals
Neoplasm Proteins
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Chiou Shin-Heng
Department of Obstetrics and Gynecology, National Taiwan University Hospital, 7 Chung-Shan South Road, Taipei 100, Taiwan.
Sheu Bor-Ching
Chang Wen-Chun
Huang Su-Cheng
Hong-Nerng Ho
Article Info
Journal
Journal of reproductive immunology
Abbr.
J Reprod Immunol
ISSN
0165-0378
Published
2005-10-00
Epub
2005-00-18
Pages
35-50
Language
English
Region
Ireland
NLM ID
8001906
Subset
IM
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