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Serum IgG Is Associated With Risk of Melanoma in the Swedish AMORIS Study
Background: Relatively little is known about the role of the humoral immune system in melanoma. Tumor infiltrating B cells in melanoma patients have been associated with increased T cell activation in tumors as well as improved patient survival. Immunoglobulins may play an important part in the anti...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828930/ https://www.ncbi.nlm.nih.gov/pubmed/31737561 http://dx.doi.org/10.3389/fonc.2019.01095 |
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author | Kessler, Anna Sollie, Sam Karagiannis, Sophia N. Walldius, Goran Hammar, Niklas Van Hemelrijck, Mieke |
author_facet | Kessler, Anna Sollie, Sam Karagiannis, Sophia N. Walldius, Goran Hammar, Niklas Van Hemelrijck, Mieke |
author_sort | Kessler, Anna |
collection | PubMed |
description | Background: Relatively little is known about the role of the humoral immune system in melanoma. Tumor infiltrating B cells in melanoma patients have been associated with increased T cell activation in tumors as well as improved patient survival. Immunoglobulins may play an important part in the anti-tumor immune response. We hypothesized that increased levels of pre-diagnostic serum Ig may be protective against melanoma development. Hence, we evaluated associations between pre-diagnostic serum markers of the immunoglobulin A (IgA), IgG and IgM, and risk of developing melanoma in the Swedish Apolipoprotein-related MORtality RISk (AMORIS) study. Methods: Study participants aged ≥20 years with baseline measurements of IgG, IgA and IgM taken between 1985 and 1996 were selected (n = 29,876). All individuals were free from melanoma at baseline and 162 study participants developed melanoma during follow up. Cox proportional hazards regression was carried out for medical cut-offs of IgA, IgG, and IgM. Results: Compared to the reference level of 6.10–14.99 g/l, we observed a positive but not significant association with risk of melanoma for those with IgG levels <6.10 g/L [HR: 1.05 (95% CI 0.39–2.86)] and an inverse association for those with IgG levels ≥15.00 g/L [HR: 0.60 (95% CI 0.34–1.05); P(trend) = 0.08]. No associations with serum IgA or IgM were identified. Conclusions: The humoral response might provide a protective role against the development of melanoma, mediated through IgG. Further research is needed to characterize this response which may be exploitable for development of future therapies. |
format | Online Article Text |
id | pubmed-6828930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68289302019-11-15 Serum IgG Is Associated With Risk of Melanoma in the Swedish AMORIS Study Kessler, Anna Sollie, Sam Karagiannis, Sophia N. Walldius, Goran Hammar, Niklas Van Hemelrijck, Mieke Front Oncol Oncology Background: Relatively little is known about the role of the humoral immune system in melanoma. Tumor infiltrating B cells in melanoma patients have been associated with increased T cell activation in tumors as well as improved patient survival. Immunoglobulins may play an important part in the anti-tumor immune response. We hypothesized that increased levels of pre-diagnostic serum Ig may be protective against melanoma development. Hence, we evaluated associations between pre-diagnostic serum markers of the immunoglobulin A (IgA), IgG and IgM, and risk of developing melanoma in the Swedish Apolipoprotein-related MORtality RISk (AMORIS) study. Methods: Study participants aged ≥20 years with baseline measurements of IgG, IgA and IgM taken between 1985 and 1996 were selected (n = 29,876). All individuals were free from melanoma at baseline and 162 study participants developed melanoma during follow up. Cox proportional hazards regression was carried out for medical cut-offs of IgA, IgG, and IgM. Results: Compared to the reference level of 6.10–14.99 g/l, we observed a positive but not significant association with risk of melanoma for those with IgG levels <6.10 g/L [HR: 1.05 (95% CI 0.39–2.86)] and an inverse association for those with IgG levels ≥15.00 g/L [HR: 0.60 (95% CI 0.34–1.05); P(trend) = 0.08]. No associations with serum IgA or IgM were identified. Conclusions: The humoral response might provide a protective role against the development of melanoma, mediated through IgG. Further research is needed to characterize this response which may be exploitable for development of future therapies. Frontiers Media S.A. 2019-10-29 /pmc/articles/PMC6828930/ /pubmed/31737561 http://dx.doi.org/10.3389/fonc.2019.01095 Text en Copyright © 2019 Kessler, Sollie, Karagiannis, Walldius, Hammar and Van Hemelrijck. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology Kessler, Anna Sollie, Sam Karagiannis, Sophia N. Walldius, Goran Hammar, Niklas Van Hemelrijck, Mieke Serum IgG Is Associated With Risk of Melanoma in the Swedish AMORIS Study |
title | Serum IgG Is Associated With Risk of Melanoma in the Swedish AMORIS Study |
title_full | Serum IgG Is Associated With Risk of Melanoma in the Swedish AMORIS Study |
title_fullStr | Serum IgG Is Associated With Risk of Melanoma in the Swedish AMORIS Study |
title_full_unstemmed | Serum IgG Is Associated With Risk of Melanoma in the Swedish AMORIS Study |
title_short | Serum IgG Is Associated With Risk of Melanoma in the Swedish AMORIS Study |
title_sort | serum igg is associated with risk of melanoma in the swedish amoris study |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6828930/ https://www.ncbi.nlm.nih.gov/pubmed/31737561 http://dx.doi.org/10.3389/fonc.2019.01095 |
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