Immunohistochemical pattern of T lymphocytes population within bilharzial-associated bladder neoplasm microenvironment

The present work aimed to investigate the cellular and immunochemical pattern of T cells population in biopsy material from chronic schistosomiasis haematobium Egyptian patients complicated with bladder cancer. Digital real-time quantitative photocytometry was applied to auto-analyze 29 stained tiss...

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Veröffentlicht in:International journal of immunopathology and pharmacology 2015-06, Vol.28 (2), p.209-217
Hauptverfasser: El-Aal, Amany Ahmed Abd, Emran, Ashraf Mohamed, Al-Antably, Abeer Said, El Saftawy, Enas Ali, Bayoumy, Ibrahim R, Hassan, Nabila Salah, Badawi, Manal
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container_title International journal of immunopathology and pharmacology
container_volume 28
creator El-Aal, Amany Ahmed Abd
Emran, Ashraf Mohamed
Al-Antably, Abeer Said
El Saftawy, Enas Ali
Bayoumy, Ibrahim R
Hassan, Nabila Salah
Badawi, Manal
description The present work aimed to investigate the cellular and immunochemical pattern of T cells population in biopsy material from chronic schistosomiasis haematobium Egyptian patients complicated with bladder cancer. Digital real-time quantitative photocytometry was applied to auto-analyze 29 stained tissue sections from cases and 17 controls using STAT4, GATA3, FOXP3, and CD8 markers specific for Th1, Th2, T regulatory, and T cytotoxic cells, respectively. Area percentage showed significant high level of GATA, followed by FOXP3 and low level of both STAT and CD8 was reported. Tissue samples from five healthy bladder tissues showed significant lower optical density (OD) values. Tissue samples from 12 non-bilharzial bladder cancers showed variable OD values, reflecting wide disparity in the control group. Our results hypothesized an exclusive pattern of T population in long standing complicated schistosomiasis haematobium. Our cases were poorly controlled by unbalanced Th1/Th2 in which Th2 was dominated. FOXP3 increased significantly, however, failed to downregulate Th2, instead, the relation between Th1 and T cytotoxic was forcibly limited by the high level of FOXP3, resulting in loss of their power in defending the host against both parasite and carcinogenic changes. These results provide more clarification for the immune evasion process played by the parasite and tumor cells under the supervision of T regulatory cells. Additionally a critical role of FOXP3 is suggested in manipulating STAT4 and CD8 in favor of malignant transformation in this life-threatening parasite.
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Digital real-time quantitative photocytometry was applied to auto-analyze 29 stained tissue sections from cases and 17 controls using STAT4, GATA3, FOXP3, and CD8 markers specific for Th1, Th2, T regulatory, and T cytotoxic cells, respectively. Area percentage showed significant high level of GATA, followed by FOXP3 and low level of both STAT and CD8 was reported. Tissue samples from five healthy bladder tissues showed significant lower optical density (OD) values. Tissue samples from 12 non-bilharzial bladder cancers showed variable OD values, reflecting wide disparity in the control group. Our results hypothesized an exclusive pattern of T population in long standing complicated schistosomiasis haematobium. Our cases were poorly controlled by unbalanced Th1/Th2 in which Th2 was dominated. FOXP3 increased significantly, however, failed to downregulate Th2, instead, the relation between Th1 and T cytotoxic was forcibly limited by the high level of FOXP3, resulting in loss of their power in defending the host against both parasite and carcinogenic changes. These results provide more clarification for the immune evasion process played by the parasite and tumor cells under the supervision of T regulatory cells. 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FOXP3 increased significantly, however, failed to downregulate Th2, instead, the relation between Th1 and T cytotoxic was forcibly limited by the high level of FOXP3, resulting in loss of their power in defending the host against both parasite and carcinogenic changes. These results provide more clarification for the immune evasion process played by the parasite and tumor cells under the supervision of T regulatory cells. 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FOXP3 increased significantly, however, failed to downregulate Th2, instead, the relation between Th1 and T cytotoxic was forcibly limited by the high level of FOXP3, resulting in loss of their power in defending the host against both parasite and carcinogenic changes. These results provide more clarification for the immune evasion process played by the parasite and tumor cells under the supervision of T regulatory cells. Additionally a critical role of FOXP3 is suggested in manipulating STAT4 and CD8 in favor of malignant transformation in this life-threatening parasite.</abstract><cop>London, England</cop><pub>SAGE Publications</pub><pmid>25926591</pmid><doi>10.1177/0394632015584733</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Aged
Aged, 80 and over
Biomarkers, Tumor - metabolism
Female
Forkhead Transcription Factors
GATA3 Transcription Factor - metabolism
Humans
Lymphocyte Count - methods
Male
Middle Aged
Schistosoma
Schistosomiasis haematobia - metabolism
Schistosomiasis haematobia - pathology
STAT4 Transcription Factor - metabolism
T-Lymphocytes, Regulatory - metabolism
T-Lymphocytes, Regulatory - pathology
Th1 Cells - metabolism
Th1 Cells - pathology
Th2 Cells - metabolism
Th2 Cells - pathology
Tumor Microenvironment - physiology
Urinary Bladder Neoplasms - metabolism
Urinary Bladder Neoplasms - pathology
title Immunohistochemical pattern of T lymphocytes population within bilharzial-associated bladder neoplasm microenvironment
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