Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2023 Mar 4;9(3):e14219.
doi: 10.1016/j.heliyon.2023.e14219. eCollection 2023 Mar.

Clinical symptoms and immune injury reflected by low CD4/CD8 ratio should increase the suspicion of HIV coinfection with tuberculosis

Affiliations

Clinical symptoms and immune injury reflected by low CD4/CD8 ratio should increase the suspicion of HIV coinfection with tuberculosis

Li Li et al. Heliyon. .

Abstract

Background: Patients who are coinfected with human immunodeficiency virus 1 (HIV) and Mycobacterium tuberculosis (TB) benefit from timely diagnosis and treatment. In the present study frequencies of CD3+, CD4+, and CD8+ T cells among peripheral blood mononuclear cells (PBMCs) of patients in the Kashi region of China infected with HIV, TB, and both HIV and TB (HIV-TB) were investigated to provide a basis for rapid identification of coinfected patients.

Methods: A total of 62 patients with HIV, TB, or HIV-TB who were first hospitalized at our institution were included in the study, as were 30 controls. PBMCs were isolated, and the frequencies of CD3+, CD4+, and CD8+ T cells were determined via flow cytometry.

Results: The frequency of CD4+ T cells and the CD4/CD8 ratio were significantly lower in the HIV-TB group than in the other three groups. In fever patients the frequency of CD4+ T cells and the CD4/CD8 ratio were significantly lower in the HIV-TB group than in the HIV group and the TB group. In patients who exhibited rapid weight loss there were no significant differences in the frequency of CD4+ T cells or the CD4/CD8 ratio between the groups. The results of treatment were compared in the HIV, TB, and HIV-TB groups after 7 days, and there were obvious improvements in the frequency of CD4+ T cells and the CD4/CD8 ratio.

Conclusion: Clinical symptoms and the degree of immune injury can heighten suspicion for HIV-TB coinfection.

Keywords: CD4+ T cells; CD4/CD8 ratio; HIV-TB coinfection.

PubMed Disclaimer

Conflict of interest statement

The authors declare no competing interests.

Figures

Fig. 1
Fig. 1
a Flow cytometry analysis of CD3+, CD4+, and CD8+ T cells. b Frequencies of CD3+, CD4+, and CD8+ T cells in each group. Notes: Δ compared with the control group; * compared with the HIV group; ΔP < 0.05, ΔΔP < 0.01,ΔΔΔP < 0.001; *P < 0.05.
Fig. 1
Fig. 1
a Flow cytometry analysis of CD3+, CD4+, and CD8+ T cells. b Frequencies of CD3+, CD4+, and CD8+ T cells in each group. Notes: Δ compared with the control group; * compared with the HIV group; ΔP < 0.05, ΔΔP < 0.01,ΔΔΔP < 0.001; *P < 0.05.
Fig. 2
Fig. 2
a Flow cytometry analysis of fever patients. b Frequency of CD4+ T cells and the CD4/CD8 ratio in fever patients. Notes: * compared with the HIV group; *p < 0.05; **p < 0.01.
Fig. 3
Fig. 3
a Flow cytometry analysis of patients with rapid weight loss. b Frequency of CD4+ T cells and the CD4/CD8 ratio in patients with rapid weight loss. Notes: * compared with the HIV group; *p < 0.05.
Fig. 4
Fig. 4
a Flow cytometry analysis in patients without fever or rapid weight loss. b Frequency of CD4+ T cells and the CD4/CD8 ratio in patients without fever or rapid weight loss. Notes: * compared with the HIV group; *p < 0.05; **p < 0.01.
Fig. 5
Fig. 5
a Flow cytometry analysis of patients before treatment. b Frequency of CD4+ T cells and the CD4/CD8 ratio in patients before treatment. Notes: * compared with the HIV group; *p < 0.05; **p < 0.01.
Fig. 6
Fig. 6
a Flow cytometry analysis in patients after treatment. b Frequency of CD4+ T cells and the CD4/CD8 ratio in patients after treatment. Notes: * compared with the HIV group; *p < 0.05; **p < 0.01.

Similar articles

Cited by

References

    1. Douek D.C., Roederer M., Koup R.A. Emerging concepts in the immunopathogenesis of AIDS. Annu. Rev. Med. 2009;60:471–484. doi: 10.1146/annurev.med.60.041807.123549. - DOI - PMC - PubMed
    1. Deeks S.G., Kitchen C.M.R., Liu L., et al. Immune activation set point during early HIV infection predicts subsequent CD4+ T-cell changes independent of viral load. Blood. 2004;104(4):942–947. doi: 10.1182/blood-2003-09-3333. - DOI - PubMed
    1. Schnappinger D., Ehrt S., Voskuil M.I., et al. Transcriptional adaptation of Mycobacterium tuberculosis within macrophages: insights into the phagosomal environment. J. Exp. Med. 2003;198(5):693–704. doi: 10.1084/jem.20030846. - DOI - PMC - PubMed
    1. Whalen C., Horsburgh C.R., Hom D., et al. Accelerated course of human immunodeficiency virus infection after tuberculosis. Am. J. Respir. Crit. Care Med. 1995;151(1):129–135. doi: 10.1164/ajrccm.151.1.7812542. - DOI - PubMed
    1. Badri M., Ehrlich R., Wood R., et al. Association between tuberculosis and HIV disease progression in a high tuberculosis prevalence area. Int. J. Tubercul. Lung Dis. 2001;5:225–232. - PubMed