Evidence map›Paper›PMID 39839096›Full record

ArticleJournal of biological methods2024

Venom immunization: IgG/IgE titers, safety, risk, and methods of the VIPRBITEM cohort.

Brian P Hanley, Gustavo Gross

Abstract read
In one paragraph

Article in Journal of biological methods, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Brian P HanleyButterfly Sciences, Davis, CA 95617, USA.
Gustavo GrossUniversity of Texas Rio Grande Valley School of Medicine, 1201 West University Drive, Edinburg, TX 78539, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: This is the first study to examine a cohort that engages in the practice of immunization with snake venoms. In this practice, either fresh wet venom or venom reconstituted from freeze-dried form is used in vaccination protocols to produce hyper-immunity to venom. Methods: This is a retrospective community-initiated collaborative research (CICR) project that collated the records of venom immunization. Records of schedules, formulations, photographs, medical records, and diaries were collated from existing practitioners and evaluated by inspection and interviews. One accidental bite was observed over 3 days, with vital signs, and photographic records of swelling taken to verify reality of the bite. Over 74 snake-genera man-years, and 24 man-years of injection data from 8 participants, for 22 species of venomous snakes from Elapidae and Viperidae are represented. Six of those participants had detailed records of date, dose and effects. Results: IgG titers to 6 venoms for 4 cohort members tested of 8 included 2 with clear hyper-immune status. IgE titers were elevated for some. In 861 injections, records showed a rate of atopy/anaphylaxis of 4.3%, an infection rate of 0.58% and an abscess rate of 1.51% . Serious adverse reactions were rare and these appeared to be linked to overly aggressive immunization schedules and formulation accidents. We note that greater cross-immunity of IgE over IgG is suggested. Two basic protocols were followed, one was an approximate one month interval, the other was one or more injection(s) per week. In 176 envenomations, 175 were without antivenom treatment, two hospitalizations occurred, and one received full antivenom treatment. Dry bites were not included in our dataset. Envenomations showed a 1.14% rate of atopy/anaphylaxis, a 0.57% rate of infection and a 1.7% rate of abscess. Conclusions: Immunization of humans to snakebite is effective, and reasonably safe with care. Injection records suggest immune cross-reactivity between ophidians within the same family, and better cross-reactivity within the same genera. A cohort participant was pronounced dead based on EEG, and then recovered without treatment. A neurotoxin case with "brain death" EEG should stay on life support for 6 weeks to allow time for the immune system to clear venom.

Indexed as

Bill HaastEnvenomationSelf-immunizationVenom immunization

Identifiers

PMID39839096
PMCPMC11744060

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Registered trials

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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.