Immune-associated cells in basal cell carcinomas of skin
Increased numbers of mast cells (MCs) and lymphocytes infiltrating in basal cell carcinomas (BCCs) have been observed. The presence of these infiltrating cells has been considered a sign of an immunologic anti‐tumor response in the host, but the relationship of these two cell populations has not bee...
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Veröffentlicht in: | Journal of cutaneous pathology 1996-04, Vol.23 (2), p.140-146 |
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description | Increased numbers of mast cells (MCs) and lymphocytes infiltrating in basal cell carcinomas (BCCs) have been observed. The presence of these infiltrating cells has been considered a sign of an immunologic anti‐tumor response in the host, but the relationship of these two cell populations has not been examined. To elucidate this possible relationship, 30 non‐ulcerated BCCs were analyzed. Frozen sections of the tumors were stained with monoclonal antibodies for Langerhans' cells, lymphocyte subsets and natural killer cells. Fluorescein isothiocynate (FITC) ‐aviclin as well as anti‐tryptase and anti‐CD45RO monoclonal antibodies were used on formalin‐fixed, paraffin‐embedded secdons for mast cell and T cell identification, respectively. B cells and natural killer cells were rarely observed in these tumors. MCs and T cells were quantified by direct enumeration and expressed as number of cells per high power field (hpf). FITC‐avidin and anti‐tryptase antibodies were equivalent in their ability to identify MCs. MC content in BCCs ranged from 1.0 to 31 cells/hpf. The number of T cells ranged from 0 to 50 cells/hpf with helper/suppressor cell ratios of 0.2 to 10. There was no correlation between helper/suppressor ratios and mast cell numbers; however, an inverse relationship was observed between the numbers of T cells and the number of mast cells in these tumors. These studies indicate that T cells and MCs are the primary immune cell populations responding to BCCs, and that decreased numbers of T cells are associated with more aggressive tumors. |
doi_str_mv | 10.1111/j.1600-0560.1996.tb01287.x |
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The presence of these infiltrating cells has been considered a sign of an immunologic anti‐tumor response in the host, but the relationship of these two cell populations has not been examined. To elucidate this possible relationship, 30 non‐ulcerated BCCs were analyzed. Frozen sections of the tumors were stained with monoclonal antibodies for Langerhans' cells, lymphocyte subsets and natural killer cells. Fluorescein isothiocynate (FITC) ‐aviclin as well as anti‐tryptase and anti‐CD45RO monoclonal antibodies were used on formalin‐fixed, paraffin‐embedded secdons for mast cell and T cell identification, respectively. B cells and natural killer cells were rarely observed in these tumors. MCs and T cells were quantified by direct enumeration and expressed as number of cells per high power field (hpf). FITC‐avidin and anti‐tryptase antibodies were equivalent in their ability to identify MCs. MC content in BCCs ranged from 1.0 to 31 cells/hpf. The number of T cells ranged from 0 to 50 cells/hpf with helper/suppressor cell ratios of 0.2 to 10. There was no correlation between helper/suppressor ratios and mast cell numbers; however, an inverse relationship was observed between the numbers of T cells and the number of mast cells in these tumors. These studies indicate that T cells and MCs are the primary immune cell populations responding to BCCs, and that decreased numbers of T cells are associated with more aggressive tumors.</description><identifier>ISSN: 0303-6987</identifier><identifier>EISSN: 1600-0560</identifier><identifier>DOI: 10.1111/j.1600-0560.1996.tb01287.x</identifier><identifier>PMID: 8721448</identifier><identifier>CODEN: JCUPBN</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>Biological and medical sciences ; Carcinoma, Basal Cell - immunology ; Carcinoma, Basal Cell - pathology ; Dermatology ; Humans ; Leukocyte Count ; Lymphocyte Count ; Lymphocytes, Tumor-Infiltrating - pathology ; Mast Cells - immunology ; Medical sciences ; Skin Neoplasms - immunology ; Skin Neoplasms - pathology ; T-Lymphocytes - immunology ; Tumors of the skin and soft tissue. 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The presence of these infiltrating cells has been considered a sign of an immunologic anti‐tumor response in the host, but the relationship of these two cell populations has not been examined. To elucidate this possible relationship, 30 non‐ulcerated BCCs were analyzed. Frozen sections of the tumors were stained with monoclonal antibodies for Langerhans' cells, lymphocyte subsets and natural killer cells. Fluorescein isothiocynate (FITC) ‐aviclin as well as anti‐tryptase and anti‐CD45RO monoclonal antibodies were used on formalin‐fixed, paraffin‐embedded secdons for mast cell and T cell identification, respectively. B cells and natural killer cells were rarely observed in these tumors. MCs and T cells were quantified by direct enumeration and expressed as number of cells per high power field (hpf). FITC‐avidin and anti‐tryptase antibodies were equivalent in their ability to identify MCs. MC content in BCCs ranged from 1.0 to 31 cells/hpf. The number of T cells ranged from 0 to 50 cells/hpf with helper/suppressor cell ratios of 0.2 to 10. There was no correlation between helper/suppressor ratios and mast cell numbers; however, an inverse relationship was observed between the numbers of T cells and the number of mast cells in these tumors. These studies indicate that T cells and MCs are the primary immune cell populations responding to BCCs, and that decreased numbers of T cells are associated with more aggressive tumors.</description><subject>Biological and medical sciences</subject><subject>Carcinoma, Basal Cell - immunology</subject><subject>Carcinoma, Basal Cell - pathology</subject><subject>Dermatology</subject><subject>Humans</subject><subject>Leukocyte Count</subject><subject>Lymphocyte Count</subject><subject>Lymphocytes, Tumor-Infiltrating - pathology</subject><subject>Mast Cells - immunology</subject><subject>Medical sciences</subject><subject>Skin Neoplasms - immunology</subject><subject>Skin Neoplasms - pathology</subject><subject>T-Lymphocytes - immunology</subject><subject>Tumors of the skin and soft tissue. Premalignant lesions</subject><issn>0303-6987</issn><issn>1600-0560</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqVkFtr3DAQhUVpSTdJf0LBhJI3bzWWrEseAsmSpoHQhtDQRzGWZNDGl8SzSzf_vnbX7HvnRYzOmTPDx9gZ8CWM9XW9BMV5zks1flirlpuKQ2H0cveOLQ7Se7bggotcWaM_smOiNeegjCqP2JHRBUhpFszcte22izkS9T7hJobMx6ahLHVZhYTNvzbzOPjU9S1S1tcZPafulH2osaH4aX5P2NO3m1-r7_n9z9u71dV97qVQPEcsVAWyDrbitQ4eveVQ6lBqKwUvMBgUqE0BFmIdRAhQaDBKoi-UtFiLE3a-z30Z-tdtpI1rE003YRf7LTltQIIuYTRe7I1-6ImGWLuXIbU4vDngbsLm1m5i4yY2bsLmZmxuNw5_nrdsqzaGw-jMadS_zDqSx6YesPOJDrYRsyqAj7bLve1PauLbfxzgVk8PIKeAfB-QaBN3hwAcnp3SQpfu949bJ8WjfLT82hnxFzyol00</recordid><startdate>199604</startdate><enddate>199604</enddate><creator>Deng, J.S.</creator><creator>Brod, B.A.</creator><creator>Saito, R.</creator><creator>Tharp, M.D.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>199604</creationdate><title>Immune-associated cells in basal cell carcinomas of skin</title><author>Deng, J.S. ; Brod, B.A. ; Saito, R. ; Tharp, M.D.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4360-aa26b14fd9b0f7dcac90157d5794302ad8a3a782191efd3dd1271864ac2649af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Biological and medical sciences</topic><topic>Carcinoma, Basal Cell - immunology</topic><topic>Carcinoma, Basal Cell - pathology</topic><topic>Dermatology</topic><topic>Humans</topic><topic>Leukocyte Count</topic><topic>Lymphocyte Count</topic><topic>Lymphocytes, Tumor-Infiltrating - pathology</topic><topic>Mast Cells - immunology</topic><topic>Medical sciences</topic><topic>Skin Neoplasms - immunology</topic><topic>Skin Neoplasms - pathology</topic><topic>T-Lymphocytes - immunology</topic><topic>Tumors of the skin and soft tissue. Premalignant lesions</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Deng, J.S.</creatorcontrib><creatorcontrib>Brod, B.A.</creatorcontrib><creatorcontrib>Saito, R.</creatorcontrib><creatorcontrib>Tharp, M.D.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of cutaneous pathology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Deng, J.S.</au><au>Brod, B.A.</au><au>Saito, R.</au><au>Tharp, M.D.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immune-associated cells in basal cell carcinomas of skin</atitle><jtitle>Journal of cutaneous pathology</jtitle><addtitle>J Cutan Pathol</addtitle><date>1996-04</date><risdate>1996</risdate><volume>23</volume><issue>2</issue><spage>140</spage><epage>146</epage><pages>140-146</pages><issn>0303-6987</issn><eissn>1600-0560</eissn><coden>JCUPBN</coden><abstract>Increased numbers of mast cells (MCs) and lymphocytes infiltrating in basal cell carcinomas (BCCs) have been observed. The presence of these infiltrating cells has been considered a sign of an immunologic anti‐tumor response in the host, but the relationship of these two cell populations has not been examined. To elucidate this possible relationship, 30 non‐ulcerated BCCs were analyzed. Frozen sections of the tumors were stained with monoclonal antibodies for Langerhans' cells, lymphocyte subsets and natural killer cells. Fluorescein isothiocynate (FITC) ‐aviclin as well as anti‐tryptase and anti‐CD45RO monoclonal antibodies were used on formalin‐fixed, paraffin‐embedded secdons for mast cell and T cell identification, respectively. B cells and natural killer cells were rarely observed in these tumors. MCs and T cells were quantified by direct enumeration and expressed as number of cells per high power field (hpf). FITC‐avidin and anti‐tryptase antibodies were equivalent in their ability to identify MCs. MC content in BCCs ranged from 1.0 to 31 cells/hpf. The number of T cells ranged from 0 to 50 cells/hpf with helper/suppressor cell ratios of 0.2 to 10. There was no correlation between helper/suppressor ratios and mast cell numbers; however, an inverse relationship was observed between the numbers of T cells and the number of mast cells in these tumors. These studies indicate that T cells and MCs are the primary immune cell populations responding to BCCs, and that decreased numbers of T cells are associated with more aggressive tumors.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>8721448</pmid><doi>10.1111/j.1600-0560.1996.tb01287.x</doi><tpages>7</tpages></addata></record> |
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subjects | Biological and medical sciences Carcinoma, Basal Cell - immunology Carcinoma, Basal Cell - pathology Dermatology Humans Leukocyte Count Lymphocyte Count Lymphocytes, Tumor-Infiltrating - pathology Mast Cells - immunology Medical sciences Skin Neoplasms - immunology Skin Neoplasms - pathology T-Lymphocytes - immunology Tumors of the skin and soft tissue. Premalignant lesions |
title | Immune-associated cells in basal cell carcinomas of skin |
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