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DOI 10.1016/j.toxicon.2024.107843

Медицинская библиотека · Toxicon : official journal of the International Society on Toxinology · 2024

The changes and the potential clinical applications of cytokines in Taiwan's major venomous snakebites patients.

Lin Chih-Chuan, Wang Chia-Cheng, Ou Yang Chun-Hsiang, Liu Chien-Chun, Yu Jau-Song, Fann Wen-Chih, Chen Yen-Chia, Shih Chia-Pang

СтатьяНаблюдательное исследованиеПеревод в очереди

Аннотация

BACKGROUND

Taiwan habu (Protobothrops mucrosquamatus), green bamboo viper (Viridovipera stejnegeri), and Taiwan cobra (Naja atra) are the most venomous snakebites in Taiwan. Patients commonly present with limb swelling but misdiagnosis rates are high, and currently available diagnostic tools are limited. This study explores the immune responses in snakebite patients to aid in differential diagnosis.

METHODS

This prospective observational study investigated the changes in cytokines in snakebite patients and their potential for diagnosis.

RESULTS

Elevated pro-inflammatory cytokines IL-6 and TNF-α were observed in all snakebite patients compared to the healthy control group. While no significant disparities were observed in humoral immune response cytokines, there were significant differences in IFN-γ levels, with significantly higher IL-10 levels in patients bitten by cobras. Patients with TNF-α levels exceeding 3.02 pg/mL were more likely to have been bitten by a cobra.

CONCLUSION

This study sheds light on the immune responses triggered by various venomous snakebites, emphasizing the potential of cytokine patterns for snakebite-type differentiation. Larger studies are needed to validate these findings for clinical use, ultimately improving snakebite diagnosis and treatment.

Для цитирования: Lin Chih-Chuan, Wang Chia-Cheng, Ou Yang Chun-Hsiang, Liu Chien-Chun, Yu Jau-Song, Fann Wen-Chih, Chen Yen-Chia, Shih Chia-Pang. The changes and the potential clinical applications of cytokines in Taiwan's major venomous snakebites patients.. Toxicon : official journal of the International Society on Toxinology. 2024. DOI: 10.1016/j.toxicon.2024.107843.

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