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DOI: 10.1055/s-0042-1759758
Cerebral toxoplasmosis with neurological co-infection in people living with AIDS/HIV: results of a prospective cohort in São Paulo, Brazil
Toxoplasmose cerebral com coinfecção neurológica em pessoas que vivem com HIV/AIDS: resultados de uma coorte prospectiva em São Paulo, BrasilAbstract
Background Concomitant neurological diseases in people living with HIV/AIDS (PLWHA) is a challenging subject that has been insufficiently evaluated by prospective clinical studies. The goal of the present study was to identify the clinical characteristics and outcomes of PLWHA with cerebral toxoplasmosis and neurological co-infections.
Methods We conducted a prospective observational cohort study at a tertiary teaching center in São Paulo, Brazil, from January to July 2017. Hospitalized PLWHA aged ≥ 18 years with cerebral toxoplasmosis were consecutively enrolled. A standardized neurological examination was performed at admission and weekly until discharge or death. Diagnosis and treatment followed institutional routines; neuroradiology, molecular diagnosis, neurosurgery, and the intensive care unit (ICU) were available. The main outcomes were neurological coinfections and in-hospital death.
Results We included 44 (4.3%) cases among 1,032 hospitalized patients. The median age was 44 (interquartile range [IQR]: 35–50) years, and 50% (n = 22) of the patients were male. The median CD4+ T lymphocyte count was of 50 (IQR: 15–94) cells/mm3. Multiple lesions on computed tomography were present in 59% of the cases. Neurological coinfections were diagnosed in 20% (n = 9) of the cases, and cytomegalovirus was the most common etiology (encephalitis: n = 3; polyradiculopathy: n = 2). Longer hospital stays (30 versus 62 days; p = 0.021) and a higher rate of ICU admissions (14% versus 44%; p = 0.045) were observed among PLWHA with neurological coinfections in comparison to those without them. The rate of in-hospital mortality was of 13.6% (n = 6) (coinfection group: 33%; no coinfection group: 8.6%; p = 0.054).
Conclusion Neurological c-infections were common among PLWHA with cerebral toxoplasmosis, and cytomegalovirus was the main copathogen. The group of PLWHA with neurological co-infections underwent longer hospital stays and more frequent intensive care unit admissions. Additionally, this group of patients tended to have higher in-hospital mortality rate.
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Resumo
Antecedentes Coinfecções neurológicas em pessoas que vivem com HIV/AIDS (PVHA) é um tema que não foi suficientemente avaliado em estudos clínicos prospectivos. Nosso objetivo foi identificar as características clínicas e os desfechos de PVHA com toxoplasmose cerebral e coinfecções neurológicas.
Métodos Estudo prospectivo de coorte observacional conduzido em um centro de ensino terciário de São Paulo, Brasil, entre janeiro e julho de 2017. Foram incluídos consecutivamente PVHA internadas com ≥ 18 anos e toxoplasmose cerebral. Realizou-se exame neurológico padronizado na admissão e semanalmente até a alta/óbito. Tanto o diagnóstico quanto o tratamento seguiram a rotina institucional; neurorradiologia, diagnóstico molecular, neurocirurgia e Unidade de Terapia Intensiva (UTI) estavam disponíveis. Os principais desfechos foram coinfecções neurológicas e óbitos hospitalares.
Resultados Incluímos 44 (4,3%) casos entre 1.032 pacientes internados. A idade mediana foi de 44 (intervalo interquartil [IIQ]: : 35–50) anos, e 50% (n = 22) dos pacientes eram do sexo masculino. A contagem mediana de linfócitos T CD4+ foi de 50 (IIQ:15–94) células/mm3. Múltiplas lesões na tomografia computadorizada foram observadas em 59% dos casos. Coinfecções neurológicas foram diagnosticadas em 20% (n = 9) dos casos, sendo o citomegalovírus a etiologia mais comum (encefalite: n = 3; polirradiculopatia: n = 2). Observou-se maior tempo de internação (26 versus 62 dias; p = 0,021) e uma taxa mais alta de admissão à UTI (14% versus 44%; p = 0,045) em PVHA com coinfecções neurológicas em comparação àquelas sem coinfecção. A mortalidade intra-hospitalar foi de 13,6% (n = 6) (grupo com coinfecções: 33% versus grupo sem coinfecção: 8,6%; p = 0,054).
Conclusão Coinfecções neurológicas foram comuns em PVHA com toxoplasmose cerebral, sendo o citomegalovírus o principal copatógeno. O grupo de PVHA com coinfecções neurológicas apresentou maior tempo de internação, maior taxa de internações na UTI, e tendência a maior taxa de mortalidade intra-hospitalar.
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INTRODUCTION
Cerebral toxoplasmosis is the main neurological disease associated with people living with HIV/AIDS (PLWHA).[1] Despite its decreasing incidence in the era of the combined antiretroviral therapy (cART), cerebral toxoplasmosis remains an important cause of hospital admission in low- and middle-income countries.[2]
The risk factors are well known, and include the prevalence of Toxoplasma gondii infection in the general population, low CD4+ T lymphocyte count, and a lack of anti-T. gondii prophylaxis.[3] Nevertheless, there are few studies on the outcomes of cerebral toxoplasmosis in PLWHA in the post-cART era, particularly in Latin America.[3]
Concomitant neurological diseases in PLWHA are challenging to treat and have not been sufficiently evaluated in prospective clinical studies. As exposure to pathogens varies by region, the incidence of coinfection and other diseases may also be influenced by the current epidemiological scenario. For example, given the high prevalence of Cryptococcus neoformans and Mycobacterium tuberculosis in India, coinfections by these pathogens are more common in this region than in Europe or North America.[4] Suspicion and timely identification of concomitant neurological diseases in PLWHA enable the provision of the appropriate treatment for these patients. The present study aimed to identify the frequency, key features, and outcomes of cerebral toxoplasmosis with neurological coinfection in PLWHA.
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METHODS
Setting
The present study was conducted at Instituto de Infectologia Emilio Ribas, a referral infectious disease hospital in the city of São Paulo, Brazil, between January 1 and August 31, 2017.
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Design
The present prospective observational cohort study on PLWHA experiencing cerebral toxoplasmosis and neurological coinfections is a sub-analysis of a study published elsewhere.[5]
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Patients
The eligible patients had HIV/AIDS with neurological complaints and were admitted to hospital. The inclusion criteria were: age ≥ 18 years; confirmed HIV diagnosis; diagnosis of cerebral toxoplasmosis during hospitalization; and diagnosis of other neurological coinfections during hospitalization. Patients were excluded if they presented exacerbation of previous neurological sequelae. The study sample was followed up until death or discharge.
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Definitions
Cerebral toxoplasmosis was defined as confirmed or probable according to the following criteria: confirmed – positive histopathological or polymerase chain reaction (PCR) of the cerebrospinal fluid (CSF) of patients with clinical and radiological improvement after 10 to 14 days of treatment; and probable – compatible clinical and radiological findings with improvement after 10 to 14 days of treatment. Neurological coinfections were defined as confirmed or probable according to clinical, neuroradiological, and CSF testing (including basic characteristics, cultures, antigen tests, and molecular techniques), along with histopathological results.[5]
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Variables
Sex, age, CD4+ T lymphocyte count, viral load, previous HIV medical history (opportunistic diseases and cART use), main and associated neurological symptoms, findings of neurological examinations, length of hospital stay, outcomes of hospitalization, and brain images obtained by computed tomography (CT) and/or magnetic resonance imaging (MRI) were recorded. Neurological diseases and etiological diagnoses during hospitalization were also documented.
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Measurements and outcomes
A neurological examination was performed on admission, and follow-up was continued weekly until death or discharge. Clinical, laboratory, and radiological data were prospectively collected. Diagnosis and treatment were based on institutional protocols, and the investigators did not influence the management of the cases. The history of CD4+ T lymphocyte count and viral load was collected using the National Network Laboratory Testing System of CD4 +/CD8+ T lymphocyte count and HIV viral load.
The outcomes of the present study included length of hospital stay, admission to the Intensive Care Unit (ICU), and in-hospital mortality in patients with concomitant neurological infections and in all patients with cerebral toxoplasmosis.
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Statistical analysis
A normality test was used to define the population distribution of the quantitative variables. Normally-distributed quantitative variables were analyzed with the Student t-test and non-normal data, with the Mann–Whitney U test. Chi-squared tests were used to analyze the qualitative variables. Variables with values of p < 0.2 were selected for binary logistic regression. Data were analyzed using Statistical Package for the Social Sciences (IBM SPSS Statistics for Windows, IBM Corp., Armonk, NY, US) software, version 22.0. Statistical significance was set at p < 0.05.
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RESULTS
General results
A total of 1,032 patients were admitted; 44 (4.3%) of them had cerebral toxoplasmosis, and their clinical and radiological characteristics are presented in [Table 1]. The median age was of 44 (interquartile range [IQR]: 35–50) years, and 22 patients (50%) were men. Only 3 (6.8%) subjects were diagnosed with HIV infection during hospitalization. A previous cART treatment was reported in 39 patients (88%). Other opportunistic diseases were diagnosed in 26 patients (59%) during hospitalization. The median CD4+ T lymphocyte count was of 50 (IQR: 15–94) cells/mm3.
Abbreviations: cART, combined antiretroviral therapy; CSF, cerebrospinal fluid; IgG, immunoglobulin G; IQR, interquartile range; ICU, Intensive Care Unit; PCR, polymerase chain reaction.
The median duration of the neurological symptoms before hospital admission was of 10 (IQR: 5–25) days. The main neurological syndrome observed was focal encephalitis (n = 27; 61%); however, 12 patients (26%) presented with diffuse encephalitis or meningoencephalitis. Multiple focal brain lesions were observed on CT in 26 patients (59%), and 8 patients (18%) were referred to the ICU.
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Etiological diagnosis and neurological coinfections
Anti-T. gondii immunoglobulin G (IgG) and immunoglobulin M (IgM) antibodies were detected in 33 patients (75%). Positive IgG and IgM were observed in 32 (96%) and 1 (3%) of the patients respectively. The CSF PCR test was available for 17 (38%) patients, and it was only positive in 3 (17%). The median time from anti-T. gondii treatment to T. gondii sample collection for PCR was of 13 (IQR: 4–25) days. Cerebral toxoplasmosis was considered confirmed in 3 (7%) and probable in 41 (93%) patients. Cerebral biopsy was only performed in 1 patient, and the diagnosis of cerebral toxoplasmosis was confirmed.
Neurological coinfections were found in 9 (20%) patients. The etiological agents in these patients were cytomegalovirus (encephalitis: 3; polyradiculopathy: 2), Treponema pallidum (meningitis: 2), and 1 case each of C. neoformans and M. tuberculosis as meningoencephalitis. In addition to clinical and basic CSF characteristics and/or neuroradiological findings, CMV was diagnosed using CSF PCR. Research laboratory testing and fluorescent treponemal antibody absorption test on CSF were used to diagnose T. pallidum, and C. neoformans was diagnosed via cryptococcal antigen test, while M. tuberculosis, via CSF PCR.
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Treatment and outcomes
Trimethoprim-sulfamethoxazole was the initial anti-T. gondii agent in 43 (97%) patients, and pyrimethamine-sulfadiazine was preferred in 3 (7%) subjects. In total, 6 (13%) patients died during hospitalization, all of sepsis due to nosocomial pneumonia.
Patients with cerebral toxoplasmosis had a median length of hospital stay of 30 (IQR: 18–51) days, 8 patients (18%) were admitted to the ICU, and 6 patients (13%) died during hospitalization ([Table 1]). Altered levels of consciousness (p < 0.0001) and ICU admission (p < 0.0001) were related to death ([Table 2]). In the binary logistic regression, altered level of consciousness (odds ratio [OR]: 37; 95% confidence interval (95%CI): 2.8–474; p = 0.006) and ICU admission (OR: 42; 95%CI: 2.9–416; p = 0.002) were associated with in-hospital mortality, while neurological coinfection showed a trend towards significant association (OR: 5.3; 95%CI: 0.86–32.99; p = 0.072).
Abbreviations: cART, combined antiretroviral therapy; ICU, Intensive Care Unit; IQR, interquartile range.
Note: Significant results appear in bold.
Patients with neurological coinfections had longer hospitalizations (26 days versus 62 days; p = 0.021) and were admitted more frequently to the ICU (14% versus 44%; p = 0.045) than the group without coinfections ([Table 3]). An analysis of the CSFs was available for 29 (65%) patients, and th results differed only in that higher protein levels were found in the neurological coinfection group (53 mg/dL versus 154 mg/dL; p = 0.04).
Abbreviations: cART, combined antiretroviral therapy; CSF, cerebrospinal fluid; ICU, Intensive Care Unit; IQR, interquartile range.
Note: Significant results appear in bold.
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DISCUSSION
In the present study, 20% of the PLWHA with cerebral toxoplasmosis had neurological coinfections, and CMV was the most common etiology. Patients with neurological coinfections had longer hospital stays and a higher rate of ICU admissions.
The profile of the patients in the present study highlights the gap between public health system infrastructure (that is, a well-structured national program including universal and free distribution of cART) and its effectiveness. Most patients in the present study had been previously diagnosed with HIV/AIDS, had received cART and prophylaxis, and had had prior opportunistic diseases. Despite the fact that almost 90% of patients are cART-experienced, barriers to retention in care and regular use of therapy indicate a loss of opportunities in this vulnerable population.
Neurological coinfections in PLWHA are challenging and usually considered uncommon. In the clinical practice, the diagnosis is commonly delayed or unnoticed. Detailed neurological evaluations on admission and during hospitalization are key to enable the timely suspicion of neurological co-infection. For example, 1 patient with advanced HIV infection showed hemiparesis and decreased visual acuity upon admission, concomitant with cerebral toxoplasmosis and CMV retinitis. Another patient with advanced HIV infection was admitted due to headache and seizures, but developed worsening headache, nausea, and vomiting after a week of anti-T. gondii treatment. He was subsequently diagnosed with cerebral toxoplasmosis and cryptococcal meningitis. Seminal neuropathological postmortem studies have shown the importance of neurological co-infections in PLWHA. Lang et al.[6] demonstrated that 14% of their patients had neurological coinfections, and Jellinger et al.[7] found a 20% coinfection rate. It is plausible that neurological coinfections are misdiagnosed in the clinical practice, which can affect the outcomes of PLWHA. Few clinical studies have been conducted on concomitant neurological infections. Variables such as the rate of exposure to pathogens in the general population and availability of appropriate diagnostic tools may explain, in part, the presence of coinfections. Yang et al.[8] evaluated CSF samples using multiplex PCR and found a coinfection rate of 24%; Cryptococcus spp. and CMV were the two most common etiologies in the coinfection group. Siddiqi et al.[9] also evaluated multiple pathogens in CSF samples and found a 21% coinfection rate. In this study,[9] the main copathogens were C. spp. and the Epstein-Barr virus. Here, 20% of the patients with cerebral toxoplasmosis had neurological coinfections, and CMV was the most common pathogen. In all of these cases, molecular identification associated with neurological syndromes confirmed the presence of a concomitant neurological disease caused by CMV. This finding differs from the possibility of a non-pathogenic concomitant virus presence in the CSF.[9]
Interestingly, the main coinfection with cerebral toxoplasmosis was caused by CMV. We have often observed this in patients admitted to our institution: CMV was the third most common pathogen associated with symptomatic neuroinfection in a general neurological cohort.[5] Our patients presented with approximately a decade of HIV infection diagnosis before admission and often had previous irregular use of cART, highlighting a prolonged and advanced HIV disease. Immune pathways regulate CMV reactivation, such as the Th1 response triggered by presentation of antigens through major histocompatibility complex-II (MHC-II) to CD4+ helper T cells,[10] and cytotoxic CD8+ T cell response.[11] Nevertheless, both of them are impaired in prolonged HIV infection.[11] Therefore, it is expected that patients will present with a high prevalence of CMV infections and end-organ diseases, not only in the neurological AIDS scenario but also in other clinical syndromes, as previously reported by our group.[12] Finally, the use of molecular diagnostic resources was fully available at our institution, and its importance has been demonstrated in CMV infection antemortem diagnoses, which were only established by CMV culture and biopsy.[13] [14]
The identification of concomitant neurological infections in PLWHA has important consequences at both the individual and public health levels. In the present study, patients with more than one neurological infection showed a trend towards higher in-hospital mortality rates. Nevertheless, this result may be attributed to the small sample size. Despite this limitation, our results show an association between neurological coinfections and longer hospitalization and/or ICU admissions. The management of HIV/AIDS has a high cost to the public health system compared to that of other chronic diseases.[15] Longer hospitalizations and more frequent ICU admissions in PLWHA for concomitant neurological infections increase this cost burden, which is particularly complicated in economically-constrained settings.
In the present study, the mortality rate was of 13%. The factors related to poor prognosis included ICU admission and altered levels of consciousness upon hospital admission. The PLWHA admitted to hospital facilities experience variable outcomes according to the setting. Li et al.[16] reported a mortality rate of 11% in China, which is similar to our results. Interestingly, they developed a prognosis score based on seven characteristics: fever, dizziness, memory deficits, disorders of consciousness, time of symptoms, CD4+ T cell count, and patchy lesion presence, with an accuracy of 91.1%. Nevertheless, Luma et al.[17] found a 30% mortality in Cameroon with the major factors relating to death including altered level of consciousness, focal signs, neck stiffness, or low CD4+ T cell count. Soneville et al.[18] evaluated patients admitted to the ICU only due to cerebral toxoplasmosis and found a mortality rate of 24%; Glasgow Coma Score and low CD4+ T cell count were related to poor prognosis. Despite the epidemiological and resource divergences among these studies, altered levels of consciousness were consistently associated with outcomes in patients with cerebral toxoplasmosis.
The present study has some limitations. First, only one center was included, with a relatively low number of patients. However, detailed prospective clinical and laboratory evaluations were performed. Second, the outcomes were evaluated exclusively during hospitalization; therefore, a long-term evaluation was impossible. However, the prolonged periods of hospitalization and follow-up strengthen our results. Finally, most patients were diagnosed with probable cerebral toxoplasmosis, a category commonly used in the clinical practice. Few patients had molecular confirmation of cerebral toxoplasmosis in their CSF samples, and the resultant interval between the initiation of anti-T. gondii treatment and CSF collection was prolonged. This delay may be partially due, to the contraindication of lumbar puncture CSF collection secondary to mass effect at hospital admission and routine practices at the time the study was carried out, using clinical and radiological parameters for the management of cerebral toxoplasmosis.
In conclusion, neurological coinfections were common in PLWHA with cerebral toxoplasmosis, and CMV was the main copathogen. The group of PLWHA with neurological coinfections had longer hospitalizations and a higher rate of ICU admissions. Coinfection is likely associated with increased mortality; however, further investigation is necessary. Our findings highlight the impact of neurological coinfections and their potential implications in the management and outcome of cerebral toxoplasmosis in PLWHA.
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Conflict of Interest
The authors have no conflict of interests to declare.
Authors' Contributions
JPMT: data collection and analysis, manuscript writing; JEV: manuscript writing and final review.
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References
- 1 Ford N, Shubber Z, Meintjes G. et al. Causes of hospital admission among people living with HIV worldwide: a systematic review and meta-analysis. Lancet HIV 2015; 2 (10) e438-e444
- 2 Imran D, Estiasari R, Maharani K. et al. Presentation, etiology, and outcome of brain infections in an Indonesian hospital: A cohort study. Neurol Clin Pract 2018; 8 (05) 379-388
- 3 Martin-Iguacel R, Ahlström MG, Touma M. et al. Incidence, presentation and outcome of toxoplasmosis in HIV infected in the combination antiretroviral therapy era. J Infect 2017; 75 (03) 263-273
- 4 Satishchandra P, Nalini A, Gourie-Devi M. et al. Profile of neurologic disorders associated with HIV/AIDS from Bangalore, south India (1989-96). Indian J Med Res 2000; 111: 14-23
- 5 Telles JP, Fernandes R, Barros TD. et al. Neurological manifestations in people living with HIV/AIDS in the late cART era: a prospective observational study at a tertiary healthcare center in São Paulo, Brazil. HIV Res Clin Pract 2021; 22 (04) 87-95
- 6 Lang W, Miklossy J, Deruaz JP. et al. Neuropathology of the acquired immune deficiency syndrome (AIDS): a report of 135 consecutive autopsy cases from Switzerland. Acta Neuropathol 1989; 77 (04) 379-390
- 7 Jellinger KA, Setinek U, Drlicek M, Böhm G, Steurer A, Lintner F. Neuropathology and general autopsy findings in AIDS during the last 15 years. Acta Neuropathol 2000; 100 (02) 213-220
- 8 Yang R, Zhang H, Xiong Y. et al. Molecular diagnosis of central nervous system opportunistic infections and mortality in HIV-infected adults in Central China. AIDS Res Ther 2017; 14: 24
- 9 Siddiqi OK, Ghebremichael M, Dang X. et al. Molecular diagnosis of central nervous system opportunistic infections in HIV-infected Zambian adults. Clin Infect Dis 2014; 58 (12) 1771-1777
- 10 Griffiths P, Reeves M. Pathogenesis of human cytomegalovirus in the immunocompromised host. Nat Rev Microbiol 2021; 19 (12) 759-773
- 11 Collins DR, Gaiha GD, Walker BD. CD8+ T cells in HIV control, cure and prevention. Nat Rev Immunol 2020; 20 (08) 471-482
- 12 Telles JP, de Andrade Perez M, Marcusso R, Correa K, Teixeira RFA, Tobias WM. Hemophagocytic syndrome in patients living with HIV: a retrospective study. Ann Hematol 2019; 98 (01) 67-72
- 13 Cinque P, Vago L, Brytting M. et al. Cytomegalovirus infection of the central nervous system in patients with AIDS: diagnosis by DNA amplification from cerebrospinal fluid. J Infect Dis 1992; 166 (06) 1408-1411
- 14 Gallant JE, Moore RD, Richman DD, Keruly J, Chaisson RE. The Zidovudine Epidemiology Study Group. Incidence and natural history of cytomegalovirus disease in patients with advanced human immunodeficiency virus disease treated with zidovudine. J Infect Dis 1992; 166 (06) 1223-1227
- 15 Settumba SN, Sweeney S, Seeley J. et al. The health system burden of chronic disease care: an estimation of provider costs of selected chronic diseases in Uganda. Trop Med Int Health 2015; 20 (06) 781-790
- 16 Li Y, Zeng YM, Liu M. et al. Development of a risk scoring system for prognostication in HIV-related toxoplasma encephalitis. BMC Infect Dis 2020; 20 (01) 923
- 17 Luma HN, Tchaleu BC, Mapoure YN. et al. Toxoplasma encephalitis in HIV/AIDS patients admitted to the Douala general hospital between 2004 and 2009: a cross sectional study. BMC Res Notes 2013; 6: 146
- 18 Sonneville R, Schmidt M, Messika J. et al. Neurologic outcomes and adjunctive steroids in HIV patients with severe cerebral toxoplasmosis. Neurology 2012; 79 (17) 1762-1766
Address for correspondence
Publikationsverlauf
Eingereicht: 14. Januar 2022
Angenommen: 21. Mai 2022
Artikel online veröffentlicht:
14. März 2023
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References
- 1 Ford N, Shubber Z, Meintjes G. et al. Causes of hospital admission among people living with HIV worldwide: a systematic review and meta-analysis. Lancet HIV 2015; 2 (10) e438-e444
- 2 Imran D, Estiasari R, Maharani K. et al. Presentation, etiology, and outcome of brain infections in an Indonesian hospital: A cohort study. Neurol Clin Pract 2018; 8 (05) 379-388
- 3 Martin-Iguacel R, Ahlström MG, Touma M. et al. Incidence, presentation and outcome of toxoplasmosis in HIV infected in the combination antiretroviral therapy era. J Infect 2017; 75 (03) 263-273
- 4 Satishchandra P, Nalini A, Gourie-Devi M. et al. Profile of neurologic disorders associated with HIV/AIDS from Bangalore, south India (1989-96). Indian J Med Res 2000; 111: 14-23
- 5 Telles JP, Fernandes R, Barros TD. et al. Neurological manifestations in people living with HIV/AIDS in the late cART era: a prospective observational study at a tertiary healthcare center in São Paulo, Brazil. HIV Res Clin Pract 2021; 22 (04) 87-95
- 6 Lang W, Miklossy J, Deruaz JP. et al. Neuropathology of the acquired immune deficiency syndrome (AIDS): a report of 135 consecutive autopsy cases from Switzerland. Acta Neuropathol 1989; 77 (04) 379-390
- 7 Jellinger KA, Setinek U, Drlicek M, Böhm G, Steurer A, Lintner F. Neuropathology and general autopsy findings in AIDS during the last 15 years. Acta Neuropathol 2000; 100 (02) 213-220
- 8 Yang R, Zhang H, Xiong Y. et al. Molecular diagnosis of central nervous system opportunistic infections and mortality in HIV-infected adults in Central China. AIDS Res Ther 2017; 14: 24
- 9 Siddiqi OK, Ghebremichael M, Dang X. et al. Molecular diagnosis of central nervous system opportunistic infections in HIV-infected Zambian adults. Clin Infect Dis 2014; 58 (12) 1771-1777
- 10 Griffiths P, Reeves M. Pathogenesis of human cytomegalovirus in the immunocompromised host. Nat Rev Microbiol 2021; 19 (12) 759-773
- 11 Collins DR, Gaiha GD, Walker BD. CD8+ T cells in HIV control, cure and prevention. Nat Rev Immunol 2020; 20 (08) 471-482
- 12 Telles JP, de Andrade Perez M, Marcusso R, Correa K, Teixeira RFA, Tobias WM. Hemophagocytic syndrome in patients living with HIV: a retrospective study. Ann Hematol 2019; 98 (01) 67-72
- 13 Cinque P, Vago L, Brytting M. et al. Cytomegalovirus infection of the central nervous system in patients with AIDS: diagnosis by DNA amplification from cerebrospinal fluid. J Infect Dis 1992; 166 (06) 1408-1411
- 14 Gallant JE, Moore RD, Richman DD, Keruly J, Chaisson RE. The Zidovudine Epidemiology Study Group. Incidence and natural history of cytomegalovirus disease in patients with advanced human immunodeficiency virus disease treated with zidovudine. J Infect Dis 1992; 166 (06) 1223-1227
- 15 Settumba SN, Sweeney S, Seeley J. et al. The health system burden of chronic disease care: an estimation of provider costs of selected chronic diseases in Uganda. Trop Med Int Health 2015; 20 (06) 781-790
- 16 Li Y, Zeng YM, Liu M. et al. Development of a risk scoring system for prognostication in HIV-related toxoplasma encephalitis. BMC Infect Dis 2020; 20 (01) 923
- 17 Luma HN, Tchaleu BC, Mapoure YN. et al. Toxoplasma encephalitis in HIV/AIDS patients admitted to the Douala general hospital between 2004 and 2009: a cross sectional study. BMC Res Notes 2013; 6: 146
- 18 Sonneville R, Schmidt M, Messika J. et al. Neurologic outcomes and adjunctive steroids in HIV patients with severe cerebral toxoplasmosis. Neurology 2012; 79 (17) 1762-1766