Evidence map›Paper›PMID 41070330›Full record

ArticlePakistan journal of medical sciences2025

Genetic polymorphism of CCR5 (59029A/G) and CCR2 (-64I A/G) promoters in HIV infected patients.

Aafshar Khalid, Romeeza Tahir, Shah Jahan, Hasnain Javed

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Article in Pakistan journal of medical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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1citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Aafshar KhalidAafshar Khalid, M.Phil. Department of Immunology, University of Health Sciences, Lahore, Pakistan.
Romeeza TahirRomeeza Tahir, Ph.D. Department of Immunology, University of Health Sciences, Lahore, Pakistan.
Shah JahanShah Jahan, Ph.D. Institute of Allied Health Sciences, University of Health Sciences, Lahore, Pakistan.
Hasnain JavedHasnain Javed, Ph.D. Provincial Public Health Reference Lab, Punjab AIDS Control Program Lahore, Lahore, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Objective: Human immunodeficiency virus (HIV) is responsible for acquired immunodeficiency syndrome (AIDS), which is the final stage of infection by HIV. This study investigated the role of the CCR5-59029A/G and CCR2-64IA/G polymorphisms in HIV susceptibility in a local Pakistani population. These two chemokine receptors facilitate HIV entry into host cells, making them key genetic markers for understanding the disease progression. Methodology: This case-control study was conducted at the Laboratory of Immunology, University of Health Sciences (UHS), Lahore from July 2022 till March 2023. Blood specimens were collected of 60 newly diagnosed HIV-infected patients from Provincial Public Health Reference Lab Lahore and 60 healthy controls. PCR was followed by restriction fragment length polymorphism (RFLP) analysis with gene-specific primers and enzymes (Bsp1286I and FokI). Results: The CCR5-59029A/G polymorphism was wild-type across all participants, with no mutations detected. For the CCR2-64IA/G mutation, a minor frequency of 3.34% was observed in healthy controls, whereas no mutations were found in HIV-positive individuals. These results suggest that neither the CCR5-59029A/G nor CCR2-64IA/G polymorphisms are linked to HIV susceptibility in this population, with both groups showing a high prevalence of the wild-type forms. Conclusion: CCR5-59029A/G and CCR2-64IA/G SNPs did not appear to influence susceptibility in this local Pakistani population. This work underscores the regional variability of genetic factors in HIV research and highlights the need for further investigation of other possible contributors to HIV resistance.

Indexed as

AIDSCCR2(-64I)CCR5(59029A/G)CD4+T cellHIV

Identifiers

PMID41070330
PMCPMC12505919

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