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Long-term course of anti-factor VIII antibody in patients with hemophilia A at a single center

BACKGROUND: Immune tolerance induction (ITI) can reduce inhibitors against factor VIII concentrates by 70-80%. In this study, we elucidated the characteristics of inhibitors and attempted to determine the proper indications and timing for ITI. METHODS: Subjects included hemophilia A patients registe...

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Autores principales: Yoo, Ki Young, Joo, Sang Chun, Choi, Yong Mook
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828527/
https://www.ncbi.nlm.nih.gov/pubmed/27104190
http://dx.doi.org/10.5045/br.2016.51.1.37
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author Yoo, Ki Young
Joo, Sang Chun
Choi, Yong Mook
author_facet Yoo, Ki Young
Joo, Sang Chun
Choi, Yong Mook
author_sort Yoo, Ki Young
collection PubMed
description BACKGROUND: Immune tolerance induction (ITI) can reduce inhibitors against factor VIII concentrates by 70-80%. In this study, we elucidated the characteristics of inhibitors and attempted to determine the proper indications and timing for ITI. METHODS: Subjects included hemophilia A patients registered at the Korea Hemophilia Foundation from 1991 through 2014. Inhibitors were classified as persistent and transient. Patients were classified into groups according to peak inhibitor titer: low (<2 BU/mL), moderate (2 to <5 BU/mL), high (5 to <10 BU/mL), and very high titer (≥10 BU/mL). RESULTS: Overall, 350 (21.4%) of 1,634 hemophilia A patients developed inhibitors at least once. Of these, 100 (6.1%) and 250 (15.3%) patients developed persistent and transient inhibitors, respectively. For transient inhibitors, the median peak titer was 1.0 BU/mL, persistent for median of 11.0 months (10.0, 8.0, 13.0, and 19.0 months in the low, moderate, high, and very high titer transient inhibitor groups, respectively). Overall, 95.8% (215), 72.2% (17), 52.4% (21), and 21.7% (97) of patients in the low, moderate, high, and very high titer groups became inhibitor-negative spontaneously, without ITI. CONCLUSION: Given the spontaneous disappearance of inhibitors and high cost of ITI, it is worthwhile to postpone ITI for 11 months unless the peak inhibitor titer is greater than 10 BU/mL.
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spelling pubmed-48285272016-04-21 Long-term course of anti-factor VIII antibody in patients with hemophilia A at a single center Yoo, Ki Young Joo, Sang Chun Choi, Yong Mook Blood Res Original Article BACKGROUND: Immune tolerance induction (ITI) can reduce inhibitors against factor VIII concentrates by 70-80%. In this study, we elucidated the characteristics of inhibitors and attempted to determine the proper indications and timing for ITI. METHODS: Subjects included hemophilia A patients registered at the Korea Hemophilia Foundation from 1991 through 2014. Inhibitors were classified as persistent and transient. Patients were classified into groups according to peak inhibitor titer: low (<2 BU/mL), moderate (2 to <5 BU/mL), high (5 to <10 BU/mL), and very high titer (≥10 BU/mL). RESULTS: Overall, 350 (21.4%) of 1,634 hemophilia A patients developed inhibitors at least once. Of these, 100 (6.1%) and 250 (15.3%) patients developed persistent and transient inhibitors, respectively. For transient inhibitors, the median peak titer was 1.0 BU/mL, persistent for median of 11.0 months (10.0, 8.0, 13.0, and 19.0 months in the low, moderate, high, and very high titer transient inhibitor groups, respectively). Overall, 95.8% (215), 72.2% (17), 52.4% (21), and 21.7% (97) of patients in the low, moderate, high, and very high titer groups became inhibitor-negative spontaneously, without ITI. CONCLUSION: Given the spontaneous disappearance of inhibitors and high cost of ITI, it is worthwhile to postpone ITI for 11 months unless the peak inhibitor titer is greater than 10 BU/mL. Korean Society of Hematology; Korean Society of Blood and Marrow Transplantation; Korean Society of Pediatric Hematology-Oncology; Korean Society on Thrombosis and Hemostasis 2016-03 2016-03-25 /pmc/articles/PMC4828527/ /pubmed/27104190 http://dx.doi.org/10.5045/br.2016.51.1.37 Text en © 2016 Korean Society of Hematology http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yoo, Ki Young
Joo, Sang Chun
Choi, Yong Mook
Long-term course of anti-factor VIII antibody in patients with hemophilia A at a single center
title Long-term course of anti-factor VIII antibody in patients with hemophilia A at a single center
title_full Long-term course of anti-factor VIII antibody in patients with hemophilia A at a single center
title_fullStr Long-term course of anti-factor VIII antibody in patients with hemophilia A at a single center
title_full_unstemmed Long-term course of anti-factor VIII antibody in patients with hemophilia A at a single center
title_short Long-term course of anti-factor VIII antibody in patients with hemophilia A at a single center
title_sort long-term course of anti-factor viii antibody in patients with hemophilia a at a single center
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4828527/
https://www.ncbi.nlm.nih.gov/pubmed/27104190
http://dx.doi.org/10.5045/br.2016.51.1.37
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