FOXP3 and CD25 double staining antibody cocktails identify regulatory T cells in different types of tumor tissues using tissue microarrays.


Journal

Annals of diagnostic pathology
ISSN: 1532-8198
Titre abrégé: Ann Diagn Pathol
Pays: United States
ID NLM: 9800503

Informations de publication

Date de publication:
Feb 2019
Historique:
received: 29 10 2018
accepted: 20 11 2018
pubmed: 7 12 2018
medline: 14 6 2019
entrez: 4 12 2018
Statut: ppublish

Résumé

Regulatory T cells (Tregs) are CD4+ T cells that express CD25 and transcription factor Forkhead box P3 (FOXP3), and Tregs play a central role in regulation of tumor immunity. FOXP3 immunohistochemistry has been widely used to study Tregs in paraffin embedded tissue, and flow cytometry using fresh tissue has been used to identify FOXP3+/CD25+ double positive Tregs. In our study, we validated the FOXP3/CD25 double staining antibody cocktails for detecting Tregs in paraffin-embedded tissue. Tissue microarrays (TMA) included 115 malignant tumors, 3 ovarian mucinous borderline tumors and 15 benign tissues. Digital image analysis was performed using ImageJ software. Our results showed that FOXP3/CD25 double positive lymphocytes, a subset of FOXP3+ lymphocytes, accounted for variable percentage of the total FOXP3+ lymphocytes and they were positively correlated with FOXP3+ cell counts. Tumors from different sites had variable FOXP3+/CD25+ and FOXP3+ lymphocyte counts. Tumors from lung, head & neck and colon had more and renal cell carcinoma had minimal FOXP3+/CD25+ and FOXP3+ lymphocytes. In conclusion, FOXP3/CD25 double staining antibody cocktails can be easily applied to paraffin-embedded tissue, and FOXP3+/CD25+ Tregs count was positively correlated with FOPX3+ Tregs count but they were not interchangeable. We recommend using CD25/FOXP3 double staining for studying Tregs in tumor tissue.

Identifiants

pubmed: 30502715
pii: S1092-9134(18)30343-5
doi: 10.1016/j.anndiagpath.2018.11.005
pii:
doi:

Substances chimiques

Antibodies 0
Biomarkers 0
FOXP3 protein, human 0
Forkhead Transcription Factors 0
IL2RA protein, human 0
Interleukin-2 Receptor alpha Subunit 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

67-70

Informations de copyright

Copyright © 2018 Elsevier Inc. All rights reserved.

Auteurs

Xinmin Liu (X)

Department of Pathology, University of Texas McGovern Medical School, Houston, TX, 77030, United States of America; Department of Gynecology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.

Xiaohong Wang (X)

Department of Pathology, University of Texas McGovern Medical School, Houston, TX, 77030, United States of America.

Jianmin Ding (J)

Department of Pathology, University of Texas McGovern Medical School, Houston, TX, 77030, United States of America.

Yan Gao (Y)

Department of Pathology, University of Texas McGovern Medical School, Houston, TX, 77030, United States of America.

Yiming Zhao (Y)

Department of Gynecology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.

Ruihua Zhao (R)

Department of Gynecology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.

Qigang Sun (Q)

Department of Hepatobiliary and Pancreatic Surgery, Hainan General Hospital, No. 19 Xiuhua Road, Xiuying District, Haikou, Hainan Province 570311, China.

Songlin Zhang (S)

Department of Pathology, University of Texas McGovern Medical School, Houston, TX, 77030, United States of America. Electronic address: Songlin.Zhang@uth.tmc.edu.

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Classifications MeSH