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Response of Severe EV71-Infected Patients to Hyperimmune Plasma Treatment: A Pilot Study

Hand, foot, and mouth disease (HFMD) is highly prevalent in East and Southeast Asia. It particularly affects children under five years of age. The most common causative agents are coxsackieviruses A6 and A16, and enterovirus A71 (EV71). The clinical presentation is usually mild and self-limited, but...

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Autores principales: Techasaensiri, Chonnamet, Wongsa, Artit, Puthanakit, Thanyawee, Chokephaibulkit, Kulkanya, Chotpitayasunondh, Tawee, Charoonruangrit, Ubonwon, Sombatnimitsakul, Somjai, Puthavathana, Pilaipan, Lerdsamran, Hatairat, Auewarakul, Prasert, Tassaneetrithep, Boonrat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161181/
https://www.ncbi.nlm.nih.gov/pubmed/34069574
http://dx.doi.org/10.3390/pathogens10050625
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author Techasaensiri, Chonnamet
Wongsa, Artit
Puthanakit, Thanyawee
Chokephaibulkit, Kulkanya
Chotpitayasunondh, Tawee
Charoonruangrit, Ubonwon
Sombatnimitsakul, Somjai
Puthavathana, Pilaipan
Lerdsamran, Hatairat
Auewarakul, Prasert
Tassaneetrithep, Boonrat
author_facet Techasaensiri, Chonnamet
Wongsa, Artit
Puthanakit, Thanyawee
Chokephaibulkit, Kulkanya
Chotpitayasunondh, Tawee
Charoonruangrit, Ubonwon
Sombatnimitsakul, Somjai
Puthavathana, Pilaipan
Lerdsamran, Hatairat
Auewarakul, Prasert
Tassaneetrithep, Boonrat
author_sort Techasaensiri, Chonnamet
collection PubMed
description Hand, foot, and mouth disease (HFMD) is highly prevalent in East and Southeast Asia. It particularly affects children under five years of age. The most common causative agents are coxsackieviruses A6 and A16, and enterovirus A71 (EV71). The clinical presentation is usually mild and self-limited, but, in some cases, severe and fatal complications develop. To date, no specific therapy or worldwide vaccine is available. In general, viral infection invokes both antibody and cell-mediated immune responses. Passive immunity transfer can ameliorate the severe symptoms of diseases such as COVID-19, influenza, MERS, and SARS. Hyperimmune plasma (HIP) from healthy donors with high anti-EV71 neutralizing titer were used to transfuse confirmed EV71-infected children with neurological involvement (n = 6). It resulted in recovery within three days, with no neurological sequelae apparent upon examination 14 days later. Following HIP treatment, plasma chemokines were decreased, whereas anti-inflammatory and pro-inflammatory cytokines gradually increased. Interestingly, IL-6 and G-CSF levels in cerebrospinal fluid declined sharply within three days. These findings indicate that HIP has therapeutic potential for HFMD with neurological complications. However, given the small number of patients who have been treated, a larger cohort study should be undertaken. Successful outcomes would stimulate the development of anti-EV71 monoclonal antibody therapy.
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spelling pubmed-81611812021-05-29 Response of Severe EV71-Infected Patients to Hyperimmune Plasma Treatment: A Pilot Study Techasaensiri, Chonnamet Wongsa, Artit Puthanakit, Thanyawee Chokephaibulkit, Kulkanya Chotpitayasunondh, Tawee Charoonruangrit, Ubonwon Sombatnimitsakul, Somjai Puthavathana, Pilaipan Lerdsamran, Hatairat Auewarakul, Prasert Tassaneetrithep, Boonrat Pathogens Article Hand, foot, and mouth disease (HFMD) is highly prevalent in East and Southeast Asia. It particularly affects children under five years of age. The most common causative agents are coxsackieviruses A6 and A16, and enterovirus A71 (EV71). The clinical presentation is usually mild and self-limited, but, in some cases, severe and fatal complications develop. To date, no specific therapy or worldwide vaccine is available. In general, viral infection invokes both antibody and cell-mediated immune responses. Passive immunity transfer can ameliorate the severe symptoms of diseases such as COVID-19, influenza, MERS, and SARS. Hyperimmune plasma (HIP) from healthy donors with high anti-EV71 neutralizing titer were used to transfuse confirmed EV71-infected children with neurological involvement (n = 6). It resulted in recovery within three days, with no neurological sequelae apparent upon examination 14 days later. Following HIP treatment, plasma chemokines were decreased, whereas anti-inflammatory and pro-inflammatory cytokines gradually increased. Interestingly, IL-6 and G-CSF levels in cerebrospinal fluid declined sharply within three days. These findings indicate that HIP has therapeutic potential for HFMD with neurological complications. However, given the small number of patients who have been treated, a larger cohort study should be undertaken. Successful outcomes would stimulate the development of anti-EV71 monoclonal antibody therapy. MDPI 2021-05-19 /pmc/articles/PMC8161181/ /pubmed/34069574 http://dx.doi.org/10.3390/pathogens10050625 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Techasaensiri, Chonnamet
Wongsa, Artit
Puthanakit, Thanyawee
Chokephaibulkit, Kulkanya
Chotpitayasunondh, Tawee
Charoonruangrit, Ubonwon
Sombatnimitsakul, Somjai
Puthavathana, Pilaipan
Lerdsamran, Hatairat
Auewarakul, Prasert
Tassaneetrithep, Boonrat
Response of Severe EV71-Infected Patients to Hyperimmune Plasma Treatment: A Pilot Study
title Response of Severe EV71-Infected Patients to Hyperimmune Plasma Treatment: A Pilot Study
title_full Response of Severe EV71-Infected Patients to Hyperimmune Plasma Treatment: A Pilot Study
title_fullStr Response of Severe EV71-Infected Patients to Hyperimmune Plasma Treatment: A Pilot Study
title_full_unstemmed Response of Severe EV71-Infected Patients to Hyperimmune Plasma Treatment: A Pilot Study
title_short Response of Severe EV71-Infected Patients to Hyperimmune Plasma Treatment: A Pilot Study
title_sort response of severe ev71-infected patients to hyperimmune plasma treatment: a pilot study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8161181/
https://www.ncbi.nlm.nih.gov/pubmed/34069574
http://dx.doi.org/10.3390/pathogens10050625
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