4.8 Article

A Strategy for Efficient Preparation of Genus-Specific Diagnostic Antibodies for Snakebites

期刊

FRONTIERS IN IMMUNOLOGY
卷 12, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fimmu.2021.775678

关键词

snakebite envenoming; venom; antigen; immunogenicity; diagnosis

资金

  1. National Science Foundation of China [31930015]
  2. Ministry of Science and Technology of China [2018YFA0801403]
  3. Chinese Academy of Sciences [XDB31000000, KGFZD-135-17-011, SAJC202103]
  4. Science and Technology Department of Yunnan Province [202003AD150008, 2019ZF003, 202002AA100007, 202001AT070116]
  5. Science and Technology Department Guangxi Zhuang Autonomous Region [Z20200287]

向作者/读者索取更多资源

A new strategy has been developed for rapid and efficient clinical diagnosis of snakebite, which is crucial for successful treatment. By using multi-omics approaches to choose candidate antigens and preparing a double-antibody sandwich ELISA kit, high accuracy and feasibility in identifying snake venoms have been demonstrated.
As said by former United Nations Secretary-General Kofi Annan, Snakebite is the most important tropical disease you've never heard of. Listed as a priority neglected tropical disease by the World Health Organization, snakebite envenoming (SBE) kills in excess of 125,000 people per year. However, due to the complexity and overlap of snake venom compositions, few reliable venom diagnostic methods for genus-/species-specific identification, which is crucial for successful SBE therapy, are available. Here, we develop a strategy to select and prepare genus-specific snake venom antibodies, which allows rapid and efficient clinical diagnosis of snakebite. Multi-omics approaches are used to choose candidate antigens from snake venoms and identify genus-specific antigenic epitope peptide fragments (GSAEPs) with ideal immunogenicity, specificity, and spatial accessibility. Double-antibody sandwich ELISA kit was established by matching a polyclonal antibody against a natural antigen and a monoclonal antibody that was prepared by natural protein as antigen and can specifically target the GSAEPs. The kit shows the ability to accurately identify venoms from similar genera of Trimeresurus and Protobothrops with a detection limit of 6.25 ng/ml on the snake venoms and a little cross-reaction, thus proving high feasibility and applicability.

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