Occurrence of Tertiary Lymphoid Tissue Is Associated with T-Cell Infiltration and Predicts Better Prognosis in Early-Stage Colorectal Cancers
Tumor-infiltrating T lymphocytes (TIL) play a key role in the clinical outcome of human colorectal cancer; however, the dynamics of their recruitment along colorectal cancer clinical progression have not been fully elucidated. Tertiary lymphoid tissue (TLT) is an ectopic organized lymph node-like st...
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Veröffentlicht in: | Clinical cancer research 2014-04, Vol.20 (8), p.2147-2158 |
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creator | DI CARO, Giuseppe BERGOMAS, Francesca GRIZZI, Fabio DONI, Andrea BIANCHI, Paolo MALESCI, Alberto LAGHI, Luigi ALLAVENA, Paola MANTOVANI, Alberto MARCHESIL, Federica |
description | Tumor-infiltrating T lymphocytes (TIL) play a key role in the clinical outcome of human colorectal cancer; however, the dynamics of their recruitment along colorectal cancer clinical progression have not been fully elucidated. Tertiary lymphoid tissue (TLT) is an ectopic organized lymph node-like structure that typically forms at sites of chronic inflammation and is involved in adaptive immune responses. Its occurrence in cancer is sporadically documented and its role and clinical relevance is largely unknown.
The occurrence of TLT, the correlation with TILs, and the clinical relevance were evaluated retrospectively, in a cohort study involving a consecutive series of 351 patients with stage II and III colorectal cancer. The role of TLT in lymphocyte recruitment was assessed in a preclinical model of colorectal cancer.
In both human colorectal cancer and in a murine model of colorectal cancer, we identified organized TLT, highly vascularized (including high endothelial venules), and correlated with the density of CD3(+) TILs. Intravenous injection in mice of GFP splenocytes resulted in homing of lymphocytes to TLT, suggesting an active role of TLT in the recruitment of lymphocytes to tumor areas. Accordingly, TLT density and TIL infiltration correlated and were coordinated in predicting better patient's outcome among patients with stage II colorectal cancer.
We provide evidence that TLT is associated with lymphocyte infiltration in colorectal cancer, providing a pathway of recruitment for TILs. TLT cooperates with TILs in a coordinated antitumor immune response, when identifying patients with low-risk early-stage colorectal cancer, thus, representing a novel prognostic biomarker for colorectal cancer. |
doi_str_mv | 10.1158/1078-0432.CCR-13-2590 |
format | Article |
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The occurrence of TLT, the correlation with TILs, and the clinical relevance were evaluated retrospectively, in a cohort study involving a consecutive series of 351 patients with stage II and III colorectal cancer. The role of TLT in lymphocyte recruitment was assessed in a preclinical model of colorectal cancer.
In both human colorectal cancer and in a murine model of colorectal cancer, we identified organized TLT, highly vascularized (including high endothelial venules), and correlated with the density of CD3(+) TILs. Intravenous injection in mice of GFP splenocytes resulted in homing of lymphocytes to TLT, suggesting an active role of TLT in the recruitment of lymphocytes to tumor areas. Accordingly, TLT density and TIL infiltration correlated and were coordinated in predicting better patient's outcome among patients with stage II colorectal cancer.
We provide evidence that TLT is associated with lymphocyte infiltration in colorectal cancer, providing a pathway of recruitment for TILs. TLT cooperates with TILs in a coordinated antitumor immune response, when identifying patients with low-risk early-stage colorectal cancer, thus, representing a novel prognostic biomarker for colorectal cancer.</description><identifier>ISSN: 1078-0432</identifier><identifier>EISSN: 1557-3265</identifier><identifier>DOI: 10.1158/1078-0432.CCR-13-2590</identifier><identifier>PMID: 24523438</identifier><identifier>CODEN: CCREF4</identifier><language>eng</language><publisher>Philadelphia, PA: American Association for Cancer Research</publisher><subject>Aged ; Animals ; Antineoplastic agents ; Biological and medical sciences ; CD3 Complex - immunology ; CD3 Complex - metabolism ; Cells, Cultured ; Colorectal Neoplasms - immunology ; Colorectal Neoplasms - metabolism ; Colorectal Neoplasms - pathology ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Kaplan-Meier Estimate ; Lymphocyte Count ; Lymphocytes, Tumor-Infiltrating - immunology ; Lymphocytes, Tumor-Infiltrating - metabolism ; Lymphoid Tissue - immunology ; Lymphoid Tissue - metabolism ; Male ; Medical sciences ; Mice, Inbred C57BL ; Mice, Transgenic ; Microscopy, Confocal ; Multiple tumors. Solid tumors. Tumors in childhood (general aspects) ; Neoplasm Recurrence, Local ; Neoplasm Staging ; Pharmacology. Drug treatments ; Prognosis ; Proportional Hazards Models ; Retrospective Studies ; Risk Assessment - statistics & numerical data ; Risk Factors ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; T-Lymphocytes - immunology ; T-Lymphocytes - metabolism ; Tumors</subject><ispartof>Clinical cancer research, 2014-04, Vol.20 (8), p.2147-2158</ispartof><rights>2015 INIST-CNRS</rights><rights>2014 AACR.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438t-1d48de7cb9f4ab32c5b5205a85bbc427ef0758b3085cd5ca8e214097a2298cd73</citedby><cites>FETCH-LOGICAL-c438t-1d48de7cb9f4ab32c5b5205a85bbc427ef0758b3085cd5ca8e214097a2298cd73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,3356,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=28415626$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24523438$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>DI CARO, Giuseppe</creatorcontrib><creatorcontrib>BERGOMAS, Francesca</creatorcontrib><creatorcontrib>GRIZZI, Fabio</creatorcontrib><creatorcontrib>DONI, Andrea</creatorcontrib><creatorcontrib>BIANCHI, Paolo</creatorcontrib><creatorcontrib>MALESCI, Alberto</creatorcontrib><creatorcontrib>LAGHI, Luigi</creatorcontrib><creatorcontrib>ALLAVENA, Paola</creatorcontrib><creatorcontrib>MANTOVANI, Alberto</creatorcontrib><creatorcontrib>MARCHESIL, Federica</creatorcontrib><title>Occurrence of Tertiary Lymphoid Tissue Is Associated with T-Cell Infiltration and Predicts Better Prognosis in Early-Stage Colorectal Cancers</title><title>Clinical cancer research</title><addtitle>Clin Cancer Res</addtitle><description>Tumor-infiltrating T lymphocytes (TIL) play a key role in the clinical outcome of human colorectal cancer; however, the dynamics of their recruitment along colorectal cancer clinical progression have not been fully elucidated. Tertiary lymphoid tissue (TLT) is an ectopic organized lymph node-like structure that typically forms at sites of chronic inflammation and is involved in adaptive immune responses. Its occurrence in cancer is sporadically documented and its role and clinical relevance is largely unknown.
The occurrence of TLT, the correlation with TILs, and the clinical relevance were evaluated retrospectively, in a cohort study involving a consecutive series of 351 patients with stage II and III colorectal cancer. The role of TLT in lymphocyte recruitment was assessed in a preclinical model of colorectal cancer.
In both human colorectal cancer and in a murine model of colorectal cancer, we identified organized TLT, highly vascularized (including high endothelial venules), and correlated with the density of CD3(+) TILs. Intravenous injection in mice of GFP splenocytes resulted in homing of lymphocytes to TLT, suggesting an active role of TLT in the recruitment of lymphocytes to tumor areas. Accordingly, TLT density and TIL infiltration correlated and were coordinated in predicting better patient's outcome among patients with stage II colorectal cancer.
We provide evidence that TLT is associated with lymphocyte infiltration in colorectal cancer, providing a pathway of recruitment for TILs. TLT cooperates with TILs in a coordinated antitumor immune response, when identifying patients with low-risk early-stage colorectal cancer, thus, representing a novel prognostic biomarker for colorectal cancer.</description><subject>Aged</subject><subject>Animals</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>CD3 Complex - immunology</subject><subject>CD3 Complex - metabolism</subject><subject>Cells, Cultured</subject><subject>Colorectal Neoplasms - immunology</subject><subject>Colorectal Neoplasms - metabolism</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Kaplan-Meier Estimate</subject><subject>Lymphocyte Count</subject><subject>Lymphocytes, Tumor-Infiltrating - immunology</subject><subject>Lymphocytes, Tumor-Infiltrating - metabolism</subject><subject>Lymphoid Tissue - immunology</subject><subject>Lymphoid Tissue - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mice, Inbred C57BL</subject><subject>Mice, Transgenic</subject><subject>Microscopy, Confocal</subject><subject>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</subject><subject>Neoplasm Recurrence, Local</subject><subject>Neoplasm Staging</subject><subject>Pharmacology. Drug treatments</subject><subject>Prognosis</subject><subject>Proportional Hazards Models</subject><subject>Retrospective Studies</subject><subject>Risk Assessment - statistics & numerical data</subject><subject>Risk Factors</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>T-Lymphocytes - immunology</subject><subject>T-Lymphocytes - metabolism</subject><subject>Tumors</subject><issn>1078-0432</issn><issn>1557-3265</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpFkc9u1DAQhy0EoqXwCCBfkLik-O_GOZao0JVWKoLlbDn2pDXKxovHUbUPwTvjVbfl5LH0jT3z_Qh5z9kl59p85qw1DVNSXPb9j4bLRuiOvSDnXOu2kWKlX9b6iTkjbxB_M8YVZ-o1ORNKC6mkOSd_b71fcobZA00j3UIu0eUD3Rx2-_sUA91GxAXoGukVYvLRFQj0IZZ7um16mCa6nsc4lexKTDN1c6DfM4ToC9IvUArkek93c8KINM702uXp0Pws7g5on6aUwRc30d7VATK-Ja9GNyG8O50X5NfX621_02xuv637q03j69Cl4UGZAK0fulG5QQqvBy2YdkYPg1eihZG12gySGe2D9s6A4Ip1rROiMz608oJ8enx3n9OfBbDYXURft3EzpAUt17yVXdcqVlH9iPqcEDOMdp_jriqynNljEvZo2R4t25qE5dIek6h9H05fLMMOwnPXk_oKfDwBDr2bxlwVRPzPGcX1SqzkP9iTkvU</recordid><startdate>20140415</startdate><enddate>20140415</enddate><creator>DI CARO, Giuseppe</creator><creator>BERGOMAS, Francesca</creator><creator>GRIZZI, Fabio</creator><creator>DONI, Andrea</creator><creator>BIANCHI, Paolo</creator><creator>MALESCI, Alberto</creator><creator>LAGHI, Luigi</creator><creator>ALLAVENA, Paola</creator><creator>MANTOVANI, Alberto</creator><creator>MARCHESIL, Federica</creator><general>American Association for Cancer Research</general><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>20140415</creationdate><title>Occurrence of Tertiary Lymphoid Tissue Is Associated with T-Cell Infiltration and Predicts Better Prognosis in Early-Stage Colorectal Cancers</title><author>DI CARO, Giuseppe ; BERGOMAS, Francesca ; GRIZZI, Fabio ; DONI, Andrea ; BIANCHI, Paolo ; MALESCI, Alberto ; LAGHI, Luigi ; ALLAVENA, Paola ; MANTOVANI, Alberto ; MARCHESIL, Federica</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c438t-1d48de7cb9f4ab32c5b5205a85bbc427ef0758b3085cd5ca8e214097a2298cd73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aged</topic><topic>Animals</topic><topic>Antineoplastic agents</topic><topic>Biological and medical sciences</topic><topic>CD3 Complex - immunology</topic><topic>CD3 Complex - metabolism</topic><topic>Cells, Cultured</topic><topic>Colorectal Neoplasms - immunology</topic><topic>Colorectal Neoplasms - metabolism</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Kaplan-Meier Estimate</topic><topic>Lymphocyte Count</topic><topic>Lymphocytes, Tumor-Infiltrating - immunology</topic><topic>Lymphocytes, Tumor-Infiltrating - metabolism</topic><topic>Lymphoid Tissue - immunology</topic><topic>Lymphoid Tissue - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Mice, Inbred C57BL</topic><topic>Mice, Transgenic</topic><topic>Microscopy, Confocal</topic><topic>Multiple tumors. Solid tumors. Tumors in childhood (general aspects)</topic><topic>Neoplasm Recurrence, Local</topic><topic>Neoplasm Staging</topic><topic>Pharmacology. Drug treatments</topic><topic>Prognosis</topic><topic>Proportional Hazards Models</topic><topic>Retrospective Studies</topic><topic>Risk Assessment - statistics & numerical data</topic><topic>Risk Factors</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>T-Lymphocytes - immunology</topic><topic>T-Lymphocytes - metabolism</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>DI CARO, Giuseppe</creatorcontrib><creatorcontrib>BERGOMAS, Francesca</creatorcontrib><creatorcontrib>GRIZZI, Fabio</creatorcontrib><creatorcontrib>DONI, Andrea</creatorcontrib><creatorcontrib>BIANCHI, Paolo</creatorcontrib><creatorcontrib>MALESCI, Alberto</creatorcontrib><creatorcontrib>LAGHI, Luigi</creatorcontrib><creatorcontrib>ALLAVENA, Paola</creatorcontrib><creatorcontrib>MANTOVANI, Alberto</creatorcontrib><creatorcontrib>MARCHESIL, Federica</creatorcontrib><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>Clinical cancer research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>DI CARO, Giuseppe</au><au>BERGOMAS, Francesca</au><au>GRIZZI, Fabio</au><au>DONI, Andrea</au><au>BIANCHI, Paolo</au><au>MALESCI, Alberto</au><au>LAGHI, Luigi</au><au>ALLAVENA, Paola</au><au>MANTOVANI, Alberto</au><au>MARCHESIL, Federica</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Occurrence of Tertiary Lymphoid Tissue Is Associated with T-Cell Infiltration and Predicts Better Prognosis in Early-Stage Colorectal Cancers</atitle><jtitle>Clinical cancer research</jtitle><addtitle>Clin Cancer Res</addtitle><date>2014-04-15</date><risdate>2014</risdate><volume>20</volume><issue>8</issue><spage>2147</spage><epage>2158</epage><pages>2147-2158</pages><issn>1078-0432</issn><eissn>1557-3265</eissn><coden>CCREF4</coden><abstract>Tumor-infiltrating T lymphocytes (TIL) play a key role in the clinical outcome of human colorectal cancer; however, the dynamics of their recruitment along colorectal cancer clinical progression have not been fully elucidated. Tertiary lymphoid tissue (TLT) is an ectopic organized lymph node-like structure that typically forms at sites of chronic inflammation and is involved in adaptive immune responses. Its occurrence in cancer is sporadically documented and its role and clinical relevance is largely unknown.
The occurrence of TLT, the correlation with TILs, and the clinical relevance were evaluated retrospectively, in a cohort study involving a consecutive series of 351 patients with stage II and III colorectal cancer. The role of TLT in lymphocyte recruitment was assessed in a preclinical model of colorectal cancer.
In both human colorectal cancer and in a murine model of colorectal cancer, we identified organized TLT, highly vascularized (including high endothelial venules), and correlated with the density of CD3(+) TILs. Intravenous injection in mice of GFP splenocytes resulted in homing of lymphocytes to TLT, suggesting an active role of TLT in the recruitment of lymphocytes to tumor areas. Accordingly, TLT density and TIL infiltration correlated and were coordinated in predicting better patient's outcome among patients with stage II colorectal cancer.
We provide evidence that TLT is associated with lymphocyte infiltration in colorectal cancer, providing a pathway of recruitment for TILs. TLT cooperates with TILs in a coordinated antitumor immune response, when identifying patients with low-risk early-stage colorectal cancer, thus, representing a novel prognostic biomarker for colorectal cancer.</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>24523438</pmid><doi>10.1158/1078-0432.CCR-13-2590</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Aged Animals Antineoplastic agents Biological and medical sciences CD3 Complex - immunology CD3 Complex - metabolism Cells, Cultured Colorectal Neoplasms - immunology Colorectal Neoplasms - metabolism Colorectal Neoplasms - pathology Female Gastroenterology. Liver. Pancreas. Abdomen Humans Kaplan-Meier Estimate Lymphocyte Count Lymphocytes, Tumor-Infiltrating - immunology Lymphocytes, Tumor-Infiltrating - metabolism Lymphoid Tissue - immunology Lymphoid Tissue - metabolism Male Medical sciences Mice, Inbred C57BL Mice, Transgenic Microscopy, Confocal Multiple tumors. Solid tumors. Tumors in childhood (general aspects) Neoplasm Recurrence, Local Neoplasm Staging Pharmacology. Drug treatments Prognosis Proportional Hazards Models Retrospective Studies Risk Assessment - statistics & numerical data Risk Factors Stomach. Duodenum. Small intestine. Colon. Rectum. Anus T-Lymphocytes - immunology T-Lymphocytes - metabolism Tumors |
title | Occurrence of Tertiary Lymphoid Tissue Is Associated with T-Cell Infiltration and Predicts Better Prognosis in Early-Stage Colorectal Cancers |
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