Loading…
Oral administration of lipoteichoic acid from Lactobacillus rhamnosus GG overcomes UVB‐induced immunosuppression and impairs skin tumor growth in mice
There is increasing evidence of the relevant connection and regulation between the gut and skin immune axis. In fact, oral administration of lipoteichoic acid (LTA) from Lactobacillus rhamnosus GG (LGG) prevents the development of UV‐induced skin tumors in chronically exposed mice. Here we aim to ev...
Saved in:
Published in: | European journal of immunology 2019-11, Vol.49 (11), p.2095-2102 |
---|---|
Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c4582-82a66b5d089693c43a40de128cda8ac55324c6f42a5850cdb41eacd9ce66980d3 |
---|---|
cites | cdi_FETCH-LOGICAL-c4582-82a66b5d089693c43a40de128cda8ac55324c6f42a5850cdb41eacd9ce66980d3 |
container_end_page | 2102 |
container_issue | 11 |
container_start_page | 2095 |
container_title | European journal of immunology |
container_volume | 49 |
creator | Friedrich, Adrián D. Campo, Valeria E. Cela, Eliana M. Morelli, Adrian E. Shufesky, William J. Tckacheva, Olga A. Leoni, Juliana Paz, Mariela L. Larregina, Adriana T. González Maglio, Daniel H. |
description | There is increasing evidence of the relevant connection and regulation between the gut and skin immune axis. In fact, oral administration of lipoteichoic acid (LTA) from Lactobacillus rhamnosus GG (LGG) prevents the development of UV‐induced skin tumors in chronically exposed mice. Here we aim to evaluate whether this LTA is able to revert UV‐induced immunosuppression as a mechanism involved in its anti‐tumor effect and whether it has an immunotherapeutic effect against cutaneous squamous cell carcinoma. Using a mouse model of contact hypersensitivity, we demonstrate that LTA overcomes UV‐induced skin immunosuppression. This effect was in part achieved by modulating the phenotype of lymph node resident dendritic cells (DC) and the homing of skin migratory DC. Importantly, oral LTA reduced significantly the growth of established skin tumors once UV radiation was discontinued, demonstrating that it has a therapeutic, besides the already demonstrated preventive antitumor effect. The data presented here strongly indicates that oral administration of LTA represents a promising immunotherapeutic approach for different conditions in which the skin immune system is compromised.
Oral administration of LTA overcomes UVB‐induced immunosuppression, through increased dendritic cell homing to lymph nodes, the consequent T cell priming and, finally, CD8+ effector T cell recruitment to challenged skin. Moreover, LTA is able to reduce the growth of established UVB‐induced skin tumors. |
doi_str_mv | 10.1002/eji.201848024 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6854281</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2267408732</sourcerecordid><originalsourceid>FETCH-LOGICAL-c4582-82a66b5d089693c43a40de128cda8ac55324c6f42a5850cdb41eacd9ce66980d3</originalsourceid><addsrcrecordid>eNp9kb1uFDEURi0EIkugpEWWaGgm-H89DRJEYRO0UhpCa3ltT9bL2B7smUTpeARKno8niUcbVkBBZV_76Oje-wHwEqMTjBB563b-hCAsmUSEPQILzAluGGb4MVgghFlDWomOwLNSdgihVvD2KTiimFImabsAPy-z7qG2wUdfxqxHnyJMHez9kEbnzTZ5A7XxFnY5BbjWZkybWvf9VGDe6hBTqbfVCqYbl00KrsCrLx9-ff_ho52Ms9CHMM3QMGRXyqzXcX4dtM8Flq8-wnEKKcPrnG7HLax18MY9B0863Rf34uE8Blcfzz6fnjfry9XF6ft1YxiXpJFEC7HhFslWtNQwqhmyDhNprJbacE4JM6JjRHPJkbEbhp02tjVOiLoYS4_Bu713mDbBWeNi3UKvhuyDzncqaa_-_ol-q67TjRKSMyJxFbx5EOT0bXJlVMEX4_peR5emoggRS4bkkpKKvv4H3aUpxzqeIjWSdtkSNlPNnjI5lZJdd2gGIzVnrmrm6pB55V_9OcGB_h1yBcgeuPW9u_u_TZ19umACE3oP_wy79w</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2313979242</pqid></control><display><type>article</type><title>Oral administration of lipoteichoic acid from Lactobacillus rhamnosus GG overcomes UVB‐induced immunosuppression and impairs skin tumor growth in mice</title><source>Wiley-Blackwell Read & Publish Collection</source><creator>Friedrich, Adrián D. ; Campo, Valeria E. ; Cela, Eliana M. ; Morelli, Adrian E. ; Shufesky, William J. ; Tckacheva, Olga A. ; Leoni, Juliana ; Paz, Mariela L. ; Larregina, Adriana T. ; González Maglio, Daniel H.</creator><creatorcontrib>Friedrich, Adrián D. ; Campo, Valeria E. ; Cela, Eliana M. ; Morelli, Adrian E. ; Shufesky, William J. ; Tckacheva, Olga A. ; Leoni, Juliana ; Paz, Mariela L. ; Larregina, Adriana T. ; González Maglio, Daniel H.</creatorcontrib><description>There is increasing evidence of the relevant connection and regulation between the gut and skin immune axis. In fact, oral administration of lipoteichoic acid (LTA) from Lactobacillus rhamnosus GG (LGG) prevents the development of UV‐induced skin tumors in chronically exposed mice. Here we aim to evaluate whether this LTA is able to revert UV‐induced immunosuppression as a mechanism involved in its anti‐tumor effect and whether it has an immunotherapeutic effect against cutaneous squamous cell carcinoma. Using a mouse model of contact hypersensitivity, we demonstrate that LTA overcomes UV‐induced skin immunosuppression. This effect was in part achieved by modulating the phenotype of lymph node resident dendritic cells (DC) and the homing of skin migratory DC. Importantly, oral LTA reduced significantly the growth of established skin tumors once UV radiation was discontinued, demonstrating that it has a therapeutic, besides the already demonstrated preventive antitumor effect. The data presented here strongly indicates that oral administration of LTA represents a promising immunotherapeutic approach for different conditions in which the skin immune system is compromised.
Oral administration of LTA overcomes UVB‐induced immunosuppression, through increased dendritic cell homing to lymph nodes, the consequent T cell priming and, finally, CD8+ effector T cell recruitment to challenged skin. Moreover, LTA is able to reduce the growth of established UVB‐induced skin tumors.</description><identifier>ISSN: 0014-2980</identifier><identifier>EISSN: 1521-4141</identifier><identifier>DOI: 10.1002/eji.201848024</identifier><identifier>PMID: 31334839</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>Administration, Oral ; Animals ; Antineoplastic Agents - isolation & purification ; Antineoplastic Agents - pharmacology ; Antitumor activity ; Carcinoma, Squamous Cell - drug therapy ; Carcinoma, Squamous Cell - genetics ; Carcinoma, Squamous Cell - immunology ; Carcinoma, Squamous Cell - pathology ; Cell Movement - drug effects ; Cell Movement - immunology ; Cell Movement - radiation effects ; Contact dermatitis ; Dendritic cells ; Dendritic Cells - drug effects ; Dendritic Cells - immunology ; Dendritic Cells - pathology ; Dendritic Cells - radiation effects ; Dermatitis, Contact - genetics ; Dermatitis, Contact - immunology ; Dermatitis, Contact - pathology ; Female ; Gastrointestinal Tract - drug effects ; Gastrointestinal Tract - immunology ; Gastrointestinal Tract - pathology ; Gastrointestinal Tract - radiation effects ; Homing ; Hypersensitivity ; Immune system ; Immunosuppression ; Lactobacillus rhamnosus ; Lactobacillus rhamnosus - chemistry ; Lipopolysaccharides - isolation & purification ; Lipopolysaccharides - pharmacology ; Lipoteichoic acid ; Lymph nodes ; Lymph Nodes - drug effects ; Lymph Nodes - immunology ; Lymph Nodes - pathology ; Lymph Nodes - radiation effects ; Mice ; Mice, Inbred C57BL ; Oral administration ; Phenotypes ; probiotics ; Skin ; Skin - drug effects ; Skin - immunology ; Skin - pathology ; Skin - radiation effects ; Skin cancer ; skin diseases ; Skin Neoplasms - drug therapy ; Skin Neoplasms - genetics ; Skin Neoplasms - immunology ; Skin Neoplasms - pathology ; Squamous cell carcinoma ; Teichoic Acids - isolation & purification ; Teichoic Acids - pharmacology ; tolerance ; Tumors ; Ultraviolet radiation ; Ultraviolet Rays - adverse effects ; UV radiation</subject><ispartof>European journal of immunology, 2019-11, Vol.49 (11), p.2095-2102</ispartof><rights>2019 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>2019 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4582-82a66b5d089693c43a40de128cda8ac55324c6f42a5850cdb41eacd9ce66980d3</citedby><cites>FETCH-LOGICAL-c4582-82a66b5d089693c43a40de128cda8ac55324c6f42a5850cdb41eacd9ce66980d3</cites><orcidid>0000-0002-3150-7475</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31334839$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Friedrich, Adrián D.</creatorcontrib><creatorcontrib>Campo, Valeria E.</creatorcontrib><creatorcontrib>Cela, Eliana M.</creatorcontrib><creatorcontrib>Morelli, Adrian E.</creatorcontrib><creatorcontrib>Shufesky, William J.</creatorcontrib><creatorcontrib>Tckacheva, Olga A.</creatorcontrib><creatorcontrib>Leoni, Juliana</creatorcontrib><creatorcontrib>Paz, Mariela L.</creatorcontrib><creatorcontrib>Larregina, Adriana T.</creatorcontrib><creatorcontrib>González Maglio, Daniel H.</creatorcontrib><title>Oral administration of lipoteichoic acid from Lactobacillus rhamnosus GG overcomes UVB‐induced immunosuppression and impairs skin tumor growth in mice</title><title>European journal of immunology</title><addtitle>Eur J Immunol</addtitle><description>There is increasing evidence of the relevant connection and regulation between the gut and skin immune axis. In fact, oral administration of lipoteichoic acid (LTA) from Lactobacillus rhamnosus GG (LGG) prevents the development of UV‐induced skin tumors in chronically exposed mice. Here we aim to evaluate whether this LTA is able to revert UV‐induced immunosuppression as a mechanism involved in its anti‐tumor effect and whether it has an immunotherapeutic effect against cutaneous squamous cell carcinoma. Using a mouse model of contact hypersensitivity, we demonstrate that LTA overcomes UV‐induced skin immunosuppression. This effect was in part achieved by modulating the phenotype of lymph node resident dendritic cells (DC) and the homing of skin migratory DC. Importantly, oral LTA reduced significantly the growth of established skin tumors once UV radiation was discontinued, demonstrating that it has a therapeutic, besides the already demonstrated preventive antitumor effect. The data presented here strongly indicates that oral administration of LTA represents a promising immunotherapeutic approach for different conditions in which the skin immune system is compromised.
Oral administration of LTA overcomes UVB‐induced immunosuppression, through increased dendritic cell homing to lymph nodes, the consequent T cell priming and, finally, CD8+ effector T cell recruitment to challenged skin. Moreover, LTA is able to reduce the growth of established UVB‐induced skin tumors.</description><subject>Administration, Oral</subject><subject>Animals</subject><subject>Antineoplastic Agents - isolation & purification</subject><subject>Antineoplastic Agents - pharmacology</subject><subject>Antitumor activity</subject><subject>Carcinoma, Squamous Cell - drug therapy</subject><subject>Carcinoma, Squamous Cell - genetics</subject><subject>Carcinoma, Squamous Cell - immunology</subject><subject>Carcinoma, Squamous Cell - pathology</subject><subject>Cell Movement - drug effects</subject><subject>Cell Movement - immunology</subject><subject>Cell Movement - radiation effects</subject><subject>Contact dermatitis</subject><subject>Dendritic cells</subject><subject>Dendritic Cells - drug effects</subject><subject>Dendritic Cells - immunology</subject><subject>Dendritic Cells - pathology</subject><subject>Dendritic Cells - radiation effects</subject><subject>Dermatitis, Contact - genetics</subject><subject>Dermatitis, Contact - immunology</subject><subject>Dermatitis, Contact - pathology</subject><subject>Female</subject><subject>Gastrointestinal Tract - drug effects</subject><subject>Gastrointestinal Tract - immunology</subject><subject>Gastrointestinal Tract - pathology</subject><subject>Gastrointestinal Tract - radiation effects</subject><subject>Homing</subject><subject>Hypersensitivity</subject><subject>Immune system</subject><subject>Immunosuppression</subject><subject>Lactobacillus rhamnosus</subject><subject>Lactobacillus rhamnosus - chemistry</subject><subject>Lipopolysaccharides - isolation & purification</subject><subject>Lipopolysaccharides - pharmacology</subject><subject>Lipoteichoic acid</subject><subject>Lymph nodes</subject><subject>Lymph Nodes - drug effects</subject><subject>Lymph Nodes - immunology</subject><subject>Lymph Nodes - pathology</subject><subject>Lymph Nodes - radiation effects</subject><subject>Mice</subject><subject>Mice, Inbred C57BL</subject><subject>Oral administration</subject><subject>Phenotypes</subject><subject>probiotics</subject><subject>Skin</subject><subject>Skin - drug effects</subject><subject>Skin - immunology</subject><subject>Skin - pathology</subject><subject>Skin - radiation effects</subject><subject>Skin cancer</subject><subject>skin diseases</subject><subject>Skin Neoplasms - drug therapy</subject><subject>Skin Neoplasms - genetics</subject><subject>Skin Neoplasms - immunology</subject><subject>Skin Neoplasms - pathology</subject><subject>Squamous cell carcinoma</subject><subject>Teichoic Acids - isolation & purification</subject><subject>Teichoic Acids - pharmacology</subject><subject>tolerance</subject><subject>Tumors</subject><subject>Ultraviolet radiation</subject><subject>Ultraviolet Rays - adverse effects</subject><subject>UV radiation</subject><issn>0014-2980</issn><issn>1521-4141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><recordid>eNp9kb1uFDEURi0EIkugpEWWaGgm-H89DRJEYRO0UhpCa3ltT9bL2B7smUTpeARKno8niUcbVkBBZV_76Oje-wHwEqMTjBB563b-hCAsmUSEPQILzAluGGb4MVgghFlDWomOwLNSdgihVvD2KTiimFImabsAPy-z7qG2wUdfxqxHnyJMHez9kEbnzTZ5A7XxFnY5BbjWZkybWvf9VGDe6hBTqbfVCqYbl00KrsCrLx9-ff_ho52Ms9CHMM3QMGRXyqzXcX4dtM8Flq8-wnEKKcPrnG7HLax18MY9B0863Rf34uE8Blcfzz6fnjfry9XF6ft1YxiXpJFEC7HhFslWtNQwqhmyDhNprJbacE4JM6JjRHPJkbEbhp02tjVOiLoYS4_Bu713mDbBWeNi3UKvhuyDzncqaa_-_ol-q67TjRKSMyJxFbx5EOT0bXJlVMEX4_peR5emoggRS4bkkpKKvv4H3aUpxzqeIjWSdtkSNlPNnjI5lZJdd2gGIzVnrmrm6pB55V_9OcGB_h1yBcgeuPW9u_u_TZ19umACE3oP_wy79w</recordid><startdate>201911</startdate><enddate>201911</enddate><creator>Friedrich, Adrián D.</creator><creator>Campo, Valeria E.</creator><creator>Cela, Eliana M.</creator><creator>Morelli, Adrian E.</creator><creator>Shufesky, William J.</creator><creator>Tckacheva, Olga A.</creator><creator>Leoni, Juliana</creator><creator>Paz, Mariela L.</creator><creator>Larregina, Adriana T.</creator><creator>González Maglio, Daniel H.</creator><general>Wiley Subscription Services, Inc</general><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>7QP</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>8FD</scope><scope>FR3</scope><scope>H94</scope><scope>K9.</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3150-7475</orcidid></search><sort><creationdate>201911</creationdate><title>Oral administration of lipoteichoic acid from Lactobacillus rhamnosus GG overcomes UVB‐induced immunosuppression and impairs skin tumor growth in mice</title><author>Friedrich, Adrián D. ; Campo, Valeria E. ; Cela, Eliana M. ; Morelli, Adrian E. ; Shufesky, William J. ; Tckacheva, Olga A. ; Leoni, Juliana ; Paz, Mariela L. ; Larregina, Adriana T. ; González Maglio, Daniel H.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4582-82a66b5d089693c43a40de128cda8ac55324c6f42a5850cdb41eacd9ce66980d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><topic>Administration, Oral</topic><topic>Animals</topic><topic>Antineoplastic Agents - isolation & purification</topic><topic>Antineoplastic Agents - pharmacology</topic><topic>Antitumor activity</topic><topic>Carcinoma, Squamous Cell - drug therapy</topic><topic>Carcinoma, Squamous Cell - genetics</topic><topic>Carcinoma, Squamous Cell - immunology</topic><topic>Carcinoma, Squamous Cell - pathology</topic><topic>Cell Movement - drug effects</topic><topic>Cell Movement - immunology</topic><topic>Cell Movement - radiation effects</topic><topic>Contact dermatitis</topic><topic>Dendritic cells</topic><topic>Dendritic Cells - drug effects</topic><topic>Dendritic Cells - immunology</topic><topic>Dendritic Cells - pathology</topic><topic>Dendritic Cells - radiation effects</topic><topic>Dermatitis, Contact - genetics</topic><topic>Dermatitis, Contact - immunology</topic><topic>Dermatitis, Contact - pathology</topic><topic>Female</topic><topic>Gastrointestinal Tract - drug effects</topic><topic>Gastrointestinal Tract - immunology</topic><topic>Gastrointestinal Tract - pathology</topic><topic>Gastrointestinal Tract - radiation effects</topic><topic>Homing</topic><topic>Hypersensitivity</topic><topic>Immune system</topic><topic>Immunosuppression</topic><topic>Lactobacillus rhamnosus</topic><topic>Lactobacillus rhamnosus - chemistry</topic><topic>Lipopolysaccharides - isolation & purification</topic><topic>Lipopolysaccharides - pharmacology</topic><topic>Lipoteichoic acid</topic><topic>Lymph nodes</topic><topic>Lymph Nodes - drug effects</topic><topic>Lymph Nodes - immunology</topic><topic>Lymph Nodes - pathology</topic><topic>Lymph Nodes - radiation effects</topic><topic>Mice</topic><topic>Mice, Inbred C57BL</topic><topic>Oral administration</topic><topic>Phenotypes</topic><topic>probiotics</topic><topic>Skin</topic><topic>Skin - drug effects</topic><topic>Skin - immunology</topic><topic>Skin - pathology</topic><topic>Skin - radiation effects</topic><topic>Skin cancer</topic><topic>skin diseases</topic><topic>Skin Neoplasms - drug therapy</topic><topic>Skin Neoplasms - genetics</topic><topic>Skin Neoplasms - immunology</topic><topic>Skin Neoplasms - pathology</topic><topic>Squamous cell carcinoma</topic><topic>Teichoic Acids - isolation & purification</topic><topic>Teichoic Acids - pharmacology</topic><topic>tolerance</topic><topic>Tumors</topic><topic>Ultraviolet radiation</topic><topic>Ultraviolet Rays - adverse effects</topic><topic>UV radiation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Friedrich, Adrián D.</creatorcontrib><creatorcontrib>Campo, Valeria E.</creatorcontrib><creatorcontrib>Cela, Eliana M.</creatorcontrib><creatorcontrib>Morelli, Adrian E.</creatorcontrib><creatorcontrib>Shufesky, William J.</creatorcontrib><creatorcontrib>Tckacheva, Olga A.</creatorcontrib><creatorcontrib>Leoni, Juliana</creatorcontrib><creatorcontrib>Paz, Mariela L.</creatorcontrib><creatorcontrib>Larregina, Adriana T.</creatorcontrib><creatorcontrib>González Maglio, Daniel H.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>European journal of immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Friedrich, Adrián D.</au><au>Campo, Valeria E.</au><au>Cela, Eliana M.</au><au>Morelli, Adrian E.</au><au>Shufesky, William J.</au><au>Tckacheva, Olga A.</au><au>Leoni, Juliana</au><au>Paz, Mariela L.</au><au>Larregina, Adriana T.</au><au>González Maglio, Daniel H.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Oral administration of lipoteichoic acid from Lactobacillus rhamnosus GG overcomes UVB‐induced immunosuppression and impairs skin tumor growth in mice</atitle><jtitle>European journal of immunology</jtitle><addtitle>Eur J Immunol</addtitle><date>2019-11</date><risdate>2019</risdate><volume>49</volume><issue>11</issue><spage>2095</spage><epage>2102</epage><pages>2095-2102</pages><issn>0014-2980</issn><eissn>1521-4141</eissn><abstract>There is increasing evidence of the relevant connection and regulation between the gut and skin immune axis. In fact, oral administration of lipoteichoic acid (LTA) from Lactobacillus rhamnosus GG (LGG) prevents the development of UV‐induced skin tumors in chronically exposed mice. Here we aim to evaluate whether this LTA is able to revert UV‐induced immunosuppression as a mechanism involved in its anti‐tumor effect and whether it has an immunotherapeutic effect against cutaneous squamous cell carcinoma. Using a mouse model of contact hypersensitivity, we demonstrate that LTA overcomes UV‐induced skin immunosuppression. This effect was in part achieved by modulating the phenotype of lymph node resident dendritic cells (DC) and the homing of skin migratory DC. Importantly, oral LTA reduced significantly the growth of established skin tumors once UV radiation was discontinued, demonstrating that it has a therapeutic, besides the already demonstrated preventive antitumor effect. The data presented here strongly indicates that oral administration of LTA represents a promising immunotherapeutic approach for different conditions in which the skin immune system is compromised.
Oral administration of LTA overcomes UVB‐induced immunosuppression, through increased dendritic cell homing to lymph nodes, the consequent T cell priming and, finally, CD8+ effector T cell recruitment to challenged skin. Moreover, LTA is able to reduce the growth of established UVB‐induced skin tumors.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>31334839</pmid><doi>10.1002/eji.201848024</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-3150-7475</orcidid><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0014-2980 |
ispartof | European journal of immunology, 2019-11, Vol.49 (11), p.2095-2102 |
issn | 0014-2980 1521-4141 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6854281 |
source | Wiley-Blackwell Read & Publish Collection |
subjects | Administration, Oral Animals Antineoplastic Agents - isolation & purification Antineoplastic Agents - pharmacology Antitumor activity Carcinoma, Squamous Cell - drug therapy Carcinoma, Squamous Cell - genetics Carcinoma, Squamous Cell - immunology Carcinoma, Squamous Cell - pathology Cell Movement - drug effects Cell Movement - immunology Cell Movement - radiation effects Contact dermatitis Dendritic cells Dendritic Cells - drug effects Dendritic Cells - immunology Dendritic Cells - pathology Dendritic Cells - radiation effects Dermatitis, Contact - genetics Dermatitis, Contact - immunology Dermatitis, Contact - pathology Female Gastrointestinal Tract - drug effects Gastrointestinal Tract - immunology Gastrointestinal Tract - pathology Gastrointestinal Tract - radiation effects Homing Hypersensitivity Immune system Immunosuppression Lactobacillus rhamnosus Lactobacillus rhamnosus - chemistry Lipopolysaccharides - isolation & purification Lipopolysaccharides - pharmacology Lipoteichoic acid Lymph nodes Lymph Nodes - drug effects Lymph Nodes - immunology Lymph Nodes - pathology Lymph Nodes - radiation effects Mice Mice, Inbred C57BL Oral administration Phenotypes probiotics Skin Skin - drug effects Skin - immunology Skin - pathology Skin - radiation effects Skin cancer skin diseases Skin Neoplasms - drug therapy Skin Neoplasms - genetics Skin Neoplasms - immunology Skin Neoplasms - pathology Squamous cell carcinoma Teichoic Acids - isolation & purification Teichoic Acids - pharmacology tolerance Tumors Ultraviolet radiation Ultraviolet Rays - adverse effects UV radiation |
title | Oral administration of lipoteichoic acid from Lactobacillus rhamnosus GG overcomes UVB‐induced immunosuppression and impairs skin tumor growth in mice |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-26T01%3A03%3A33IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Oral%20administration%20of%20lipoteichoic%20acid%20from%20Lactobacillus%20rhamnosus%20GG%20overcomes%20UVB%E2%80%90induced%20immunosuppression%20and%20impairs%20skin%20tumor%20growth%20in%20mice&rft.jtitle=European%20journal%20of%20immunology&rft.au=Friedrich,%20Adri%C3%A1n%20D.&rft.date=2019-11&rft.volume=49&rft.issue=11&rft.spage=2095&rft.epage=2102&rft.pages=2095-2102&rft.issn=0014-2980&rft.eissn=1521-4141&rft_id=info:doi/10.1002/eji.201848024&rft_dat=%3Cproquest_pubme%3E2267408732%3C/proquest_pubme%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c4582-82a66b5d089693c43a40de128cda8ac55324c6f42a5850cdb41eacd9ce66980d3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2313979242&rft_id=info:pmid/31334839&rfr_iscdi=true |