Evidence map›Paper›PMID 34069574›Full record

ArticlePathogens (Basel, Switzerland)2021

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

Chonnamet Techasaensiri, Artit Wongsa, Thanyawee Puthanakit, Kulkanya Chokephaibulkit, Tawee Chotpitayasunondh, Ubonwon Charoonruangrit, Somjai Sombatnimitsakul, Pilaipan Puthavathana, Hatairat Lerdsamran, Prasert Auewarakul and 1 more

Open access · goldAbstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 40% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Advances in anti-EV-A71 drug development research.Journal of advanced research · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 5 institutions in 1 country.

Chonnamet TechasaensiriDepartment of Pediatrics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok 10400, Thailand.
Artit WongsaCenter of Research Excellence in Immunoregulation, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
Thanyawee PuthanakitDepartment of Pediatrics, Faculty of Medicine, Chulalongkorn University, Bangkok 10330, Thailand.
Kulkanya ChokephaibulkitDepartment of Pediatrics, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.ORCID 0000-0002-0140-4600
Tawee ChotpitayasunondhDepartment of Pediatrics, Queen Sirikit National Institute of Child Health, Bangkok 10400, Thailand.
Ubonwon CharoonruangritNational Blood Bank Center, Thai Red Cross, Bangkok 10330, Thailand.
Somjai SombatnimitsakulNational Blood Bank Center, Thai Red Cross, Bangkok 10330, Thailand.
Pilaipan PuthavathanaCenter for Research and Innovation, Faculty of Medical Technology, Mahidol University, Nakon Pathom 73170, Thailand.
Hatairat LerdsamranCenter for Research and Innovation, Faculty of Medical Technology, Mahidol University, Nakon Pathom 73170, Thailand.
Prasert AuewarakulDepartment of Microbiology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.ORCID 0000-0002-4745-4291
Boonrat TassaneetrithepCenter of Research Excellence in Immunoregulation, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok 10700, Thailand.
Siriraj Hospital · THMahidol University · THThai Red Cross Society · THChulalongkorn University · THQueen Sirikit National Institute of Child Health · TH

Funding

Health Systems Research Institute P-13-50146
6 · The paper itself

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.

Indexed as

EV71hand, foot, and mouth diseasehyperimmune plasma treatmentneurological complication

Identifiers

PMID34069574
PMCPMC8161181
OpenAlexW3163300096

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.