scholarly journals The effect of primary drug resistance on CD4+ cell decline and the viral load set-point in HIV-positive individuals before the start of antiretroviral therapy

AIDS ◽  
2019 ◽  
Vol 33 (2) ◽  
pp. 315-326
Author(s):  
Anna Schultze ◽  
Carlo Torti ◽  
Alessandro Cozzi-Lepri ◽  
Anne-Mieke Vandamme ◽  
Maurizio Zazzi ◽  
...  
2015 ◽  
Vol 91 (Suppl 2) ◽  
pp. A233.3-A234
Author(s):  
H Eloudyi ◽  
S Lemrabet ◽  
M Malmoussi ◽  
Z Ouagari ◽  
E Elharti ◽  
...  

Author(s):  
Vasily Bondarenko ◽  
Irina Buynevich ◽  
Andrey Holyavkin ◽  
Svetlana Goponyako ◽  
Nkolaj Burinsky

Author(s):  
Anna Panova ◽  
Vadim Testov ◽  
Grigory Kaminskiy ◽  
Anastasia Samoilova ◽  
Elena Veselova ◽  
...  

2012 ◽  
Vol 05 (05) ◽  
pp. 1250032 ◽  
Author(s):  
JIE LOU ◽  
LINGCHEN BU ◽  
ESTHER HAN ◽  
YUHUA RUAN ◽  
HUI XING ◽  
...  

We propose a mathematical model to evaluate the effect of China's "Four-Free-One-Care Policy" in MSM population in Beijing. We divided the drug resistant HIV patients into two sub-populations: primary drug resistance and secondary drug resistance. Uncertainty and sensitivity analysis based on Latin Hypercube Sampling (LHS) were used for these thresholds of our model. We find that drug-resistant HIV will spread fast in MSM population under China's current treatment policy. Especially, primary-resistant strain is very likely to dominate the HIV positive MSM individuals after 10 years. The conclusions hint that, China's outlook on HIV infections is not optimistic if sufficient kinds free second-line drugs in China cannot be put into use in the near future.


2012 ◽  
Vol 6 (1) ◽  
pp. 181-187 ◽  
Author(s):  
SE Buskin ◽  
S Zhang ◽  
CS Thibault

Primary, or transmitted, HIV antiretroviral resistance is an ongoing concern despite continuing development of new antiretroviral therapies. We examined HIV surveillance data, including both patient demographic characteristics and laboratory data, combined with HIV genotypic test results to evaluate the comprehensiveness of drug resistance surveillance, prevalence of primary drug resistance, and impact, if any, of primary resistance on population-based virological outcomes. The King County, WA Variant, Atypical, and Resistant HIV Surveillance (VARHS) system increased coverage of eligible genotypic testing – within three months of an HIV diagnosis among antiretroviral naïve individuals -- from – 15% in 2003 to 69% in 2010. VARHS under-represented females, Blacks, Native Americans, and injection drug users. Primary drug resistance was more common among males, individuals aged 20 – 29 years, men who had sex with men, and individuals with an initial CD4+ lymphocyte count of 200 cells/µL and higher. High level resistance to two or three antiretroviral classes declined over time. Over 90% of sequences were HIV-1 subtype B. The proportion of individuals with a most recent viral load (closest to April 2011) that was undetectable (<50 copies/mL) was not statistically significantly associated with primary drug resistance. This was true for both number and type of antiretroviral drug class; although small numbers of specimens with drug resistance may have limited our statistical power. In summary, although we found disparities in testing coverage and prevalence of drug resistance, we were unable to detect a significantly deleterious impact of primary drug resistance based on a most recent viral load.


2021 ◽  
Author(s):  
Carlos Henrique Valente Moreira ◽  
Tassila Salomon ◽  
Cecília S. Alencar ◽  
Thelma T. Gonçalez ◽  
Ester C. Sabino ◽  
...  

2020 ◽  
Vol 18 (3) ◽  
pp. 210-218
Author(s):  
Guolong Yu ◽  
Yan Li ◽  
Xuhe Huang ◽  
Pingping Zhou ◽  
Jin Yan ◽  
...  

Background: HIV-1 CRF55_01B was first reported in 2013. At present, no report is available regarding this new clade’s polymorphisms in its functionally critical regions protease and reverse transcriptase. Objective: To identify the diversity difference in protease and reverse transcriptase between CRF55_01B and its parental clades CRF01_AE and subtype B; and to investigate CRF55_01B’s drug resistance mutations associated with the protease inhibition and reverse transcriptase inhibition. Methods: HIV-1 RNA was extracted from plasma derived from a MSM population. The reverse transcription and nested PCR amplification were performed following our in-house PCR procedure. Genotyping and drug resistant-associated mutations and polymorphisms were identified based on polygenetic analyses and the usage of the HIV Drug Resistance Database, respectively. Results: A total of 9.24 % of the identified CRF55_01B sequences bear the primary drug resistance. CRF55_01B contains polymorphisms I13I/V, G16E and E35D that differ from those in CRF01_AE. Among the 11 polymorphisms in the RT region, seven were statistically different from CRF01_AE’s. Another three polymorphisms, R211K (98.3%), F214L (98.3%), and V245A/E (98.3 %.), were identified in the RT region and they all were statistically different with that of the subtype B. The V179E/D mutation, responsible for 100% potential low-level drug resistance, was found in all CRF55_01B sequences. Lastly, the phylogenetic analyses demonstrated 18 distinct clusters that account for 35% of the samples. Conclusions: CRF55_01B’s pol has different genetic diversity comparing to its counterpart in CRF55_01B’s parental clades. CRF55_01B has a high primary drug resistance presence and the V179E/D mutation may confer more vulnerability to drug resistance.


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