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Updated: Apr 24, 2026

Humanized NOD/SCID/IL2rγnull (hu-NSG) Mouse Model for HIV Replication and Latency Studies
Published on: January 7, 2019
SARS-CoV-2 infection disrupts the immune control status in a male HIV-1 elite controller
Chun-Yu Zhao1, Fu-Sheng Wang1, Yan-Mei Jiao2
1Department of Infectious Diseases, Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, China; Beijing Ditan Hospital, Capital Medical University, Beijing, China.
Objective:
To report a case of an HIV elite controller (EC) who developed disease progression following SARS-CoV-2 infection, characterized by the breakdown of prior immune control.
Case Presentation:
We report a case of a Chinese male EC with HIV-1 CRF01_AE and protective HLA-B*57:01, who had sustained undetectable viral load and stable CD4+ T-cell counts for over 10 years. Following SARS-CoV-2 infection, he developed persistent HIV viral rebound (peaking at 4430 copies/ml) for eight months, accompanied by a profound CD4+ T-cell decline to 174 cells/µl, and subsequently initiated antiretroviral therapy. After treatment, viral load was effectively suppressed, and immune function gradually recovered.
Conclusion:
This is the first reported case of an HIV EC losing immune control after SARS-CoV-2 infection, leading to prolonged viral rebound and severe CD4+ decline. Our observation demonstrates that elite control is conditional and can be disrupted by major immunological challenges, supporting enhanced surveillance of ECs during intercurrent infections.
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