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Talaromyces marneffei infection with IFNGR1 gene mutation in a patient with negative Anti-Interferon-γ autoantibodies
Li, Shiyang; Cao, Xianwei; Guo, Zhuxiu; Wang, Jian; Tong, Jianbo; Zhang, Zhibin.
Affiliation
  • Li, Shiyang; The First Affiliated Hospital of Nanchang University. Department of Dermatology. Nanchang. CN
  • Cao, Xianwei; The First Affiliated Hospital of Nanchang University. Department of Dermatology. Nanchang. CN
  • Guo, Zhuxiu; The First Affiliated Hospital of Nanchang University. Department of Dermatology. Nanchang. CN
  • Wang, Jian; The First Affiliated Hospital of Nanchang University. Department of Dermatology. Nanchang. CN
  • Tong, Jianbo; The First Affiliated Hospital of Nanchang University. Department of Dermatology. Nanchang. CN
  • Zhang, Zhibin; The First Affiliated Hospital of Nanchang University. Department of Dermatology. Nanchang. CN
An. bras. dermatol ; 99(2): 233-237, Mar.-Apr. 2024. graf
Article 在 En | LILACS-Express | LILACS | ID: biblio-1556844
Responsible library: BR1.1
ABSTRACT
Abstract Background Talaromyces Marneffei (TM) is a rare opportunistic pathogen that mostly infects patients with low immunity compared to those with normal immunity. It may be related to immune deficiency or genetic factors. Objective To evaluate the gene mutation of a patient infected with TM in an endemic area with negative anti-interferonautoantibodies, and negative human immunodeficiency virus (HIV) infection. Methods Extract deoxyribonucleic acid (DNA) samples from the patient's peripheral blood, detect the mutation gene by whole exome sequencing (WES), and carry out Sanger sequencing verification for the detected mutation gene. Results The authors detected a mutation in the IFNGR1 gene (NM_001363526.1) and validated the detected gene mutation using Sanger sequencing. The results showed a heterozygous mutation c.4C>T (p.L2F) located in the IFNGR1 gene (NM_001363526.1). Study limitations The mechanism of the IFNGR1 gene has not been further investigated in this study. Conclusions The IFNGR1 gene mutation may be a potential risk factor for TM infection, and the presence of anti-interferonautoantibodies can aggravate disease symptoms.
Key words

全文: 1 索引: LILACS 语言: En 期刊: An. bras. dermatol 期刊主题: DERMATOLOGIA 年: 2024 类型: Article / Project document

全文: 1 索引: LILACS 语言: En 期刊: An. bras. dermatol 期刊主题: DERMATOLOGIA 年: 2024 类型: Article / Project document