Prevalence of Naturally Occurring HIV-1 Capsid Inhibitor Resistance-Related Mutations in Antiretroviral Therapy-Naïve and -Experienced Individuals in Taiwan

被引:0
作者
Chen, Nan-Yu [1 ]
Cheng, Chien-Yu [2 ]
Lo, Shih-Hao [3 ]
Lu, Po-Liang [3 ]
Yang, Chia-Jui [4 ,5 ]
Tseng, Cheng-Yin [6 ]
Tsai, Hung-Chin [6 ,7 ]
Wu, Ting-Shu [1 ]
Hsiao, Yu-Hsiang [1 ]
Liu, Zhuo-Hao [1 ]
Ku, Stephane Wen-Wei [8 ]
机构
[1] Linkou Chang Gung Mem Hosp, 5 Fushin St, Taoyuan 33333, Taiwan
[2] Minist Hlth & Welf, Taoyuan Gen Hosp, Taoyuan, Taiwan
[3] Kaohsiung Med Univ, Chung Ho Mem Hosp, Kaohsiung, Taiwan
[4] Far Eastern Mem Hosp, New Taipei City, Taiwan
[5] Natl Yang Ming Chiao Tung Univ, Taipei, Taiwan
[6] Mackay Mem Hosp, Hsinchu, Taiwan
[7] Vet Gen Hosp, Kaohsiung, Taiwan
[8] Taipei City Hosp, Ren Ai Branch, 10 Sec 4,Renai Rd, Taipei City 106243, Taiwan
关键词
capsid inhibitor; drug resistance; HIV; lenacapavir; TRANSMITTED DRUG-RESISTANCE; FAILURE; THERAPY; NAIVE;
D O I
10.1093/ofid/ofaf028
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background It is generally believed that HIV-1 capsid inhibitor-na & iuml;ve populations are susceptible to capsid inhibitors. Moreover, conventional HIV-1 resistance genotyping does not include the CA region, leading to limited surveillance data.Methods We conducted a retrospective study to investigate the presence of mutations at positions associated with capsid inhibitor resistance before the introduction of the first HIV-1 capsid inhibitor, lenacapavir, in Taiwan. Capsid mutations at positions L56, N57, M66, Q67, K70, N74, A105, and T107 were analyzed using a local HIV-1 database that encompasses near-full-length next-generation sequencing data of both antiretroviral therapy (ART)-na & iuml;ve and -experienced individuals with HIV-1, collected between 2017 and 2023 in Northern Taiwan.Results A total of 287 CA sequences were analyzed. Mutations at positions associated with capsid inhibitor resistance were rare, found in 4.5% (7/156) of ART-na & iuml;ve and 5.3% (7/131) of ART-experienced individuals, mainly as accessory mutations or polymorphisms. Notably, a Q67H mutation was found in an ART-na & iuml;ve individual at a frequency of 26.8%, while a Q67R mutation, with unclear clinical implications, appeared at 2.8% in an ART-experienced case.Conclusions This result indicated low prevalence yet undeniable existence of naturally occurring capsid inhibitor resistance-related mutations in capsid inhibitor-na & iuml;ve individuals with HIV-1. It is generally believed that HIV-1 capsid-inhibitor na & iuml;ve populations are sensitive to capsid inhibitors. However, this study discovered that naturally occurring HIV-1 capsid inhibitor-related mutations are present in capsid inhibitor-na & iuml;ve populations.
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