Publication: Response of severe ev71-infected patients to hyperimmune plasma treatment: A pilot study
Issued Date
2021-05-01
Resource Type
ISSN
20760817
Other identifier(s)
2-s2.0-85107018523
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Mahidol University
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SCOPUS
Bibliographic Citation
Pathogens. Vol.10, No.5 (2021)
Suggested Citation
Chonnamet Techasaensiri, Artit Wongsa, Thanyawee Puthanakit, Kulkanya Chokephaibulkit, Tawee Chotpitayasunondh, Ubonwon Charoonruangrit, Somjai Sombatnimitsakul, Pilaipan Puthavathana, Hatairat Lerdsamran, Prasert Auewarakul, Boonrat Tassaneetrithep Response of severe ev71-infected patients to hyperimmune plasma treatment: A pilot study. Pathogens. Vol.10, No.5 (2021). doi:10.3390/pathogens10050625 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/76185
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Title
Response of severe ev71-infected patients to hyperimmune plasma treatment: A pilot study
Abstract
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.