Clinical and laboratory characteristic of patients with COVID-19 and HIV
S.V. MOISEEVA1, A.R. BILALOVA1, A.R. AKBEROV1, I.M. KHAERTYNOVA1, B.SH. FATKULLIN2, F.K. SIRAZIEVA3
1Kazan State Medical Academy — Branch Campus of the FSBEI FPE RMACPE MOH Russia, Kazan
2Republic Clinical Infectious Hospital named after Prof. A.F. Agafonov, Kazan
3Republic Center for Prevention and Struggle against AIDS and Infectious Diseases, Kazan
Contact details:
Moiseeva S.V. — PhD (medicine), Assistant Lecturer of the Department of Infectious Diseases
Address: 36 Butlerov St., Kazan, Russian Federation, 420012, tel.: +7-917-239-96-97, e-mail: sgerasimova.kgma@gmail.com
The purpose — to investigate the clinical and laboratory manifestations of the concurrent course of HIV and SARS-CoV-2 infections.
Material and methods. We examined 76 patients with concurrent HIV and COVID-19 (with predominant circulation of Delta and Omicron variants of the SARS-CoV-2 virus), hospitalized between January and December 2022 at the Republic Clinical Infectious Hospital named after Professor A.F. Agafonov. The patients were divided into 2 groups, those who recovered (group I) and those with a fatal outcome (group II). All patients underwent laboratory and instrumental studies in accordance with Temporary Medical Advices version 17 (December 14, 2022); the HIV viral load and CD4+ T-lymphocyte level were additionally determined. Statistical analysis was performed using StatTech v. 2.8.8 and Statistica v.10.0 software.
Results. Of the 76 patients with concurrent HIV and COVID-19 infections, 23.6% were newly diagnosed with HIV upon admission. The mortality rate in this category was 44.4%, all at stages 4B–4C. Comparative analysis of complaints from patients with concurrent infections showed that group II patients had complaints of unsteady gait and speech disturbances. Comorbid pathology was detected in 100% of patients with a fatal outcome. A significant inverse correlation was found between the level of CD4+ T-lymphocytes and the duration of SARS-CoV-2 virus shedding. Analysis of laboratory parameters during hospitalization revealed a statistically significant decrease in monocyte levels in group II patients throughout the observation period.
Conclusions. A doctor should be cautious of unsteady gait and speech disturbances in patients with coronavirus infection and HIV, which may indicate possible involvement of the central nervous system. HIV patients with secondary diseases have similar complaints to those with COVID-19, complicating the timely diagnosis of coronavirus infection, especially when they have opportunistic diseases. The duration of SARS-CoV-2 shedding in patients with immunodeficiency due to HIV infection is related to the level of CD4+ T-lymphocytes. Decreased monocyte levels are a prognostically unfavorable factor for a severe course of the disease with an adverse outcome.
Key words: COVID-19, HIV infection, duration of SARS-CoV-2 shedding, concurrent disease course, monocytes, hospitalization outcome.
(For citation: Moiseeva S.V., Bilalova A.R., Akberov A.R., Khaertynova I.M., Fatkullin B.Sh., Sirazieva F.K. Clinical and laboratory characteristic of patients with COVID-19 and HIV. Practical medicine. 2023. Vol. , № , P.)
REFERENCES
- Brown L.B., Spinelli M.A., Gandhi M. The interplay between HIV and COVID-19: summary of the data and responses to date. Curr Opin HIV AIDS, 2021, vol. 16 (1), pp. 63–73. DOI: 10.1097/COH.0000000000000659
- Forchette L., Sebastian W., Liu T. A Comprehensive Review of COVID-19 Virology, Vaccines, Variants, and Therapeutics. Curr Med Sci, 2021, vol. 41 (6), pp. 1037–1051. DOI: 10.1007/s11596-021-2395-1
- AIDS info. Interim guidance for COVID‐19 and persons with HIV COVID‐19 and persons with HIV (Interim Guidance). Feb. 22, 2022, available at: https://clinicalinfo.hiv.gov/en/guidelines/guidance-covid-19-and-people-hiv/guidance-covid-19-and-people-hiv
- Pokrovskiy V.V., Ermak T.N., Belyaeva V.V., Yurin O.G. VICh-infektsiya: klinika, diagnostika i lechenie [HIV infection: clinical picture, diagnosis and treatment]. Moscow: GEOTAR-Media, 2003. 488 p.
- Stepanova E.V., Leonova O.N., Shelomov A.S., Vinogradova T.N. New coronavirus infection (COVID-19) in patients with HIV infection. Zhurnal infektologii, 2021, vol. 13, pp. 61–69 (in Russ.). DOI: 10.22625/2072-6732-2021-13-2-61-69
- Voznesenskiy S.L., Ermak T.N., Kozhevnikova G.M., Abramova E.V. Combined secondary diseases in HIV-infected patients. Infektsionnye bolezni, 2022, vol. 20, no. 2, pp. 97–103 (in Russ.). DOI: 10.20953/1729-9225-2022-2-97-103
- Leonova O.N., Stepanova E.V., Belyakov N.A. Severe and comorbid conditions in patients with HIV infection: Analysis of adverse outcomes. VICh-infektsiya i immunosupressii, 2017, vol. 9, no. 1, pp. 55–64 (in Russ.). DOI: 10.22328/2077-9828-2017-9-1-55-64
- Jakharia N., Subramanian A.K., Shapiro A.E. COVID-19 in the Immunocompromised Host, Including People with Human Immunodeficiency Virus. Infect Dis Clin North Am, 2022, vol. 36 (2), pp. 397–421. DOI: 10.1016/j.idc.2022.01.006
- Yousaf M., Hameed M., Alsoub H., Khatib M., Jamal W., Ahmad M. COVID-19: Prolonged viral shedding in an HIV patient with literature review of risk factors for prolonged viral shedding and its implications for isolation strategies. Clin Case Rep, 2021, vol. 9 (3), pp. 1397–1401. DOI: 10.1002/ccr3.3786
- Karim F., Moosa M.Y., Gosnell B. et al. Persistent SARS-CoV-2 infection and intra-host evolution in association with advanced HIV infection. medRxiv, 2021. DOI: 10.1101/2021.06.03.21258228
- Stanevich O.V., Alekseeva E.I., Sergeeva M. et al. SARS-CoV-2 escape from cytotoxic T cells during long-term COVID-19. Nat Commun, 2023, vol. 14 (1), pp. 149. DOI: 10.1038/s41467-022-34033-x
- Shi C., Pamer E.G. Monocyte recruitment during infection and inflammation. Nat Rev Immunol, 2011, vol. 11 (11), pp. 762–774. DOI: 10.1038/nri3070
- Chen J., Wang R., Wang M., Wei G.-W. Mutations Strengthened SARS-CoV-2 Infectivity. J. Mol. Biol., 2020, vol. 432, pp. 5212–5226. DOI: 10.1016/j.jmb.2020.07.009
- Peacock T.P. et al. The furin cleavage site of SARS-CoV-2 spike protein is a key determinant for transmission due to enhanced replication in airway cells. 10.1101/2020.09.30.318311 (2020)
- Parihar A., Eubank T.D., Doseff A.I. Monocytes and macrophages regulate immunity through dynamic networks of survival and cell death. J Innate Immun, 2010, vol. 2 (3), pp. 204–215. DOI: 10.1159/000296507
- Meidaninikjeh S., Sabouni N., Marzouni H.Z. et al. Monocytes and macrophages in COVID-19: Friends and foes. Life Sci, 2021, vol. 269, p. 119010. DOI: 10.1016/j.lfs.2020.119010
- Wu A., Peng Y., Huang B. et al. Genome Composition and Divergence of the Novel Coronavirus (2019-nCoV) Originating in China. Cell Host Microbe, 2020, vol. 27 (3), pp. 325–328. Doi: 10.1016/j.chom.2020.02.001
- Paliogiannis P., Zinellu A., Scano V. et al. Laboratory test alterations in patients with COVID-19 and non COVID-19 interstitial pneumonia: a preliminary report. J Infect Dev Ctries, 2020, vol. 14 (7), pp. 685–690. DOI: 10.3855/jidc.12879
- Henry B.M., de Oliveira M.H.S., Benoit S., Plebani M., Lippi G. Hematologic, biochemical and immune biomarker abnormalities associated with severe illness and mortality in coronavirus disease 2019 (COVID-19): a meta-analysis. Clin Chem Lab Med, 2020, vol. 58 (7), pp. 1021–1028. DOI: 10.1515/cclm-2020-0369
- Andonegui-Elguera S., Taniguchi-Ponciano K., Gonzalez-Bonilla C.R. et al. Molecular Alterations Prompted by SARS-CoV-2 Infection: Induction of Hyaluronan, Glycosaminoglycan and Mucopolysaccharide Metabolism. Arch Med Res, 2020, vol. 51 (7), pp. 645–653. DOI: 10.1016/j.arcmed.2020.06.011