Literature DB >> 26026717

Immunological cross-reactivity and neutralization of the principal toxins of Naja sumatrana and related cobra venoms by a Thai polyvalent antivenom (Neuro Polyvalent Snake Antivenom).

Poh Kuan Leong1, Shin Yee Fung1, Choo Hock Tan2, Si Mui Sim2, Nget Hong Tan3.   

Abstract

The low potency of cobra antivenom has been an area of concern in immunotherapy for cobra envenomation. This study sought to investigate factors limiting the neutralizing potency of cobra antivenom, using a murine model. We examined the immunological reactivity and neutralizing potency of a Thai polyvalent antivenom against the principal toxins of Naja sumatrana (Equatorial spitting cobra) venom and two related Asiatic cobra venom α-neurotoxins. The antivenom possesses moderate neutralizing potency against phospholipases A2 (P, potency of 0.98mg/mL) and moderately weak neutralizing potency against long-chain α-neurotoxins (0.26-0.42mg/mL) but was only weakly effective in neutralizing the short-chain α-neurotoxins and cardiotoxins (0.05-0.08mg/mL). The poor neutralizing potency of the antivenom on the low molecular mass short-chain neurotoxins and cardiotoxins is presumably the main limiting factor of the efficacy of the cobra antivenom. Our results also showed that phospholipase A2, which exhibited the highest ELISA reactivity and avidity, was most effectively neutralized, whereas N. sumatrana short-chain neurotoxin, which exhibited the lowest ELISA reactivity and avidity, was least effectively neutralized by the antivenom. These observations suggest that low immunoreactivity (low ELISA reactivity and avidity) is one of the reasons for poor neutralization of the cobra venom low molecular mass toxins. Nevertheless, the overall results show that there is a lack of congruence between the immunological reactivity of the toxins toward antivenom and the effectiveness of toxin neutralization by the antivenom, indicating that there are other factors that also contribute to the weak neutralization capacity of the antivenom. Several suggestions have been put forward to overcome the low efficacy of the cobra antivenom. The use of a 'proper-mix' formulation of cobra venoms as immunogen, whereby the immunogen mixture used for hyperimmunization contains a mix of various types of α-neurotoxins and cardiotoxins in sufficient amount, may also help to improve the efficacy and broaden the neutralization spectrum of the antivenom.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cobra venom toxins; Cross neutralization; Immunological activity; Polyvalent antivenom

Mesh:

Substances:

Year:  2015        PMID: 26026717     DOI: 10.1016/j.actatropica.2015.05.020

Source DB:  PubMed          Journal:  Acta Trop        ISSN: 0001-706X            Impact factor:   3.112


  20 in total

1.  Venom and Purified Toxins of the Spectacled Cobra (Naja naja) from Pakistan: Insights into Toxicity and Antivenom Neutralization.

Authors:  Kin Ying Wong; Choo Hock Tan; Nget Hong Tan
Journal:  Am J Trop Med Hyg       Date:  2016-03-28       Impact factor: 2.345

Review 2.  A Quest for a Universal Plasma-Derived Antivenom Against All Elapid Neurotoxic Snake Venoms.

Authors:  Kavi Ratanabanangkoon
Journal:  Front Immunol       Date:  2021-04-23       Impact factor: 7.561

3.  Assessing SABU (Serum Anti Bisa Ular), the sole Indonesian antivenom: A proteomic analysis and neutralization efficacy study.

Authors:  Choo Hock Tan; Jia Lee Liew; Kae Yi Tan; Nget Hong Tan
Journal:  Sci Rep       Date:  2016-11-21       Impact factor: 4.379

4.  Exploration of immunoglobulin transcriptomes from mice immunized with three-finger toxins and phospholipases A2 from the Central American coral snake, Micrurus nigrocinctus.

Authors:  Andreas H Laustsen; Mikael Engmark; Christopher Clouser; Sonia Timberlake; Francois Vigneault; José María Gutiérrez; Bruno Lomonte
Journal:  PeerJ       Date:  2017-01-24       Impact factor: 2.984

5.  A novel in vitro potency assay of antisera against Thai Naja kaouthia based on nicotinic acetylcholine receptor binding.

Authors:  Kavi Ratanabanangkoon; Pavinee Simsiriwong; Kritsada Pruksaphon; Kae Yi Tan; Sukanya Eursakun; Choo Hock Tan; Bunkuea Chantrathonkul; Wongsakorn Wongwadhunyoo; Sirida Youngchim; Nget Hong Tan
Journal:  Sci Rep       Date:  2017-08-17       Impact factor: 4.379

6.  Cross-Neutralisation of In Vitro Neurotoxicity of Asian and Australian Snake Neurotoxins and Venoms by Different Antivenoms.

Authors:  Anjana Silva; Wayne C Hodgson; Geoffrey K Isbister
Journal:  Toxins (Basel)       Date:  2016-10-18       Impact factor: 4.546

7.  The Snake with the Scorpion's Sting: Novel Three-Finger Toxin Sodium Channel Activators from the Venom of the Long-Glanded Blue Coral Snake (Calliophis bivirgatus).

Authors:  Daryl C Yang; Jennifer R Deuis; Daniel Dashevsky; James Dobson; Timothy N W Jackson; Andreas Brust; Bing Xie; Ivan Koludarov; Jordan Debono; Iwan Hendrikx; Wayne C Hodgson; Peter Josh; Amanda Nouwens; Gregory J Baillie; Timothy J C Bruxner; Paul F Alewood; Kelvin Kok Peng Lim; Nathaniel Frank; Irina Vetter; Bryan G Fry
Journal:  Toxins (Basel)       Date:  2016-10-18       Impact factor: 4.546

8.  Comparative venom gland transcriptomics of Naja kaouthia (monocled cobra) from Malaysia and Thailand: elucidating geographical venom variation and insights into sequence novelty.

Authors:  Kae Yi Tan; Choo Hock Tan; Lawan Chanhome; Nget Hong Tan
Journal:  PeerJ       Date:  2017-04-05       Impact factor: 2.984

9.  Neutralization of the Principal Toxins from the Venoms of Thai Naja kaouthia and Malaysian Hydrophis schistosus: Insights into Toxin-Specific Neutralization by Two Different Antivenoms.

Authors:  Kae Yi Tan; Choo Hock Tan; Shin Yee Fung; Nget Hong Tan
Journal:  Toxins (Basel)       Date:  2016-03-26       Impact factor: 4.546

10.  Analysis of the efficacy of Taiwanese freeze-dried neurotoxic antivenom against Naja kaouthia, Naja siamensis and Ophiophagus hannah through proteomics and animal model approaches.

Authors:  Chien-Chun Liu; Chen-Hsien You; Po-Jung Wang; Jau-Song Yu; Guo-Jen Huang; Chien-Hsin Liu; Wen-Chin Hsieh; Chih-Chuan Lin
Journal:  PLoS Negl Trop Dis       Date:  2017-12-15
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