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2031. False-positive Serologic Results attributable to IVIG therapy
BACKGROUND: Intravenous immunoglobulin (IVIG) is used to treat an increasing number of conditions including hematologic, rheumatologic and immunodeficiency diseases. The immunomodulatory effects can be life-saving, however recent administration can complicate diagnostics when patients later present...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253139/ http://dx.doi.org/10.1093/ofid/ofy210.1687 |
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author | Hanson, Kimberly E Gabriel, Nielsen Mchardy, Ian Hoffmann, Wesley Cohen, Stuart H Welch, Ryan Couturier, Marc Roger Thompson, George R |
author_facet | Hanson, Kimberly E Gabriel, Nielsen Mchardy, Ian Hoffmann, Wesley Cohen, Stuart H Welch, Ryan Couturier, Marc Roger Thompson, George R |
author_sort | Hanson, Kimberly E |
collection | PubMed |
description | BACKGROUND: Intravenous immunoglobulin (IVIG) is used to treat an increasing number of conditions including hematologic, rheumatologic and immunodeficiency diseases. The immunomodulatory effects can be life-saving, however recent administration can complicate diagnostics when patients later present with symptoms necessitating serologic testing. We evaluated the serologic profile of IVIG for commonly ordered infectious diseases serologies. METHODS: Patients were enrolled if they received and were naïve to IVIG therapy. Blood was drawn prior to IVIG and 72–96 hours post-infusion. All samples were tested for: Bartonella, Coccidioides, Brucella, Histoplasma, Coxiella, West Nile, St. Louis, California, Eastern, and Western Encephalitis, Lyme, Dengue, HSV 1 and 2, Chikungunya, cytomegalovirus, varicella zoster, Epstein-Barr and Toxoplasma by standard methodologies (ARUP, Salt Lake City, UT). Pre- and post-infusion antibody concentrations were evaluated to determine the potential false-positive rate of serologic testing. RESULTS: Seven patients received IVIG (renal transplant rejection, two patients; Guillain–Barre syndrome, three patients; bone marrow transplant, two patients). Six of seven patients receiving IVIG had at least one evaluated serology become positive 72 hours after IVIG infusion. Antibodies for CMV, HSV-2, and EBV early antigen D turned positive in three patients. Antibodies for WNV, Coccidioides IgG, and Histoplasma yeast IgG became positive in two patients.Finally, antibodies for HSV-1 and -2, and EBV nuclear antigen each turned positive in one patient. Patients received between 20 and 112.5 g. Of the three patients who received more than 100 g of IVIG, two had at least four serologies turn positive. Of the patients who received <100 g (20–50 g), none had >3 turn positive (P < 0.05). One patient had three serologies turn negative (Coccidioides, HSV 2, and EBV Early D) after infusion of 36.5 g of IVIG, with none turning positive. CONCLUSION: Use of IVIG has increased significantly over the past decade; however, the potential pitfalls in serologic diagnostics associated with receipt of IVIG have not been studied systematically and is likely a confounder in serologic diagnostics causing both false-positive and false-negative results. We found a number of screening and diagnostic serologies can be artificially altered after infusion of IVIG. DISCLOSURES: All authors: No reported disclosures. |
format | Online Article Text |
id | pubmed-6253139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62531392018-11-28 2031. False-positive Serologic Results attributable to IVIG therapy Hanson, Kimberly E Gabriel, Nielsen Mchardy, Ian Hoffmann, Wesley Cohen, Stuart H Welch, Ryan Couturier, Marc Roger Thompson, George R Open Forum Infect Dis Abstracts BACKGROUND: Intravenous immunoglobulin (IVIG) is used to treat an increasing number of conditions including hematologic, rheumatologic and immunodeficiency diseases. The immunomodulatory effects can be life-saving, however recent administration can complicate diagnostics when patients later present with symptoms necessitating serologic testing. We evaluated the serologic profile of IVIG for commonly ordered infectious diseases serologies. METHODS: Patients were enrolled if they received and were naïve to IVIG therapy. Blood was drawn prior to IVIG and 72–96 hours post-infusion. All samples were tested for: Bartonella, Coccidioides, Brucella, Histoplasma, Coxiella, West Nile, St. Louis, California, Eastern, and Western Encephalitis, Lyme, Dengue, HSV 1 and 2, Chikungunya, cytomegalovirus, varicella zoster, Epstein-Barr and Toxoplasma by standard methodologies (ARUP, Salt Lake City, UT). Pre- and post-infusion antibody concentrations were evaluated to determine the potential false-positive rate of serologic testing. RESULTS: Seven patients received IVIG (renal transplant rejection, two patients; Guillain–Barre syndrome, three patients; bone marrow transplant, two patients). Six of seven patients receiving IVIG had at least one evaluated serology become positive 72 hours after IVIG infusion. Antibodies for CMV, HSV-2, and EBV early antigen D turned positive in three patients. Antibodies for WNV, Coccidioides IgG, and Histoplasma yeast IgG became positive in two patients.Finally, antibodies for HSV-1 and -2, and EBV nuclear antigen each turned positive in one patient. Patients received between 20 and 112.5 g. Of the three patients who received more than 100 g of IVIG, two had at least four serologies turn positive. Of the patients who received <100 g (20–50 g), none had >3 turn positive (P < 0.05). One patient had three serologies turn negative (Coccidioides, HSV 2, and EBV Early D) after infusion of 36.5 g of IVIG, with none turning positive. CONCLUSION: Use of IVIG has increased significantly over the past decade; however, the potential pitfalls in serologic diagnostics associated with receipt of IVIG have not been studied systematically and is likely a confounder in serologic diagnostics causing both false-positive and false-negative results. We found a number of screening and diagnostic serologies can be artificially altered after infusion of IVIG. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2018-11-26 /pmc/articles/PMC6253139/ http://dx.doi.org/10.1093/ofid/ofy210.1687 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | Abstracts Hanson, Kimberly E Gabriel, Nielsen Mchardy, Ian Hoffmann, Wesley Cohen, Stuart H Welch, Ryan Couturier, Marc Roger Thompson, George R 2031. False-positive Serologic Results attributable to IVIG therapy |
title | 2031. False-positive Serologic Results attributable to IVIG therapy |
title_full | 2031. False-positive Serologic Results attributable to IVIG therapy |
title_fullStr | 2031. False-positive Serologic Results attributable to IVIG therapy |
title_full_unstemmed | 2031. False-positive Serologic Results attributable to IVIG therapy |
title_short | 2031. False-positive Serologic Results attributable to IVIG therapy |
title_sort | 2031. false-positive serologic results attributable to ivig therapy |
topic | Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6253139/ http://dx.doi.org/10.1093/ofid/ofy210.1687 |
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