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      SARS-CoV-2 pandemic expanding in sub-Saharan Africa: Considerations for COVID-19 in people living with HIV

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      a , b , c , * , d , e
      EClinicalMedicine
      The Author(s). Published by Elsevier Ltd.

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          Abstract

          In December 2019, a novel coronavirus, SARS-CoV-2, started a global pandemic of respiratory illness, termed COVID-19 [1]. The spectrum of COVID-19 has ranged from a mild, self-limiting respiratory tract illness to severe progressive pneumonia, multi-organ failure, and death [2]. Older patients and those with a weaker immune system appear to have a greater risk of death [3]. Thus far, the vast majority of deaths from COVID-19 have occurred in Italy, China, Iran, and Spain—all Northern hemisphere countries with good health care resources and a low HIV prevalence. After the SARS-CoV-2 pandemic reached sub-Saharan Africa, COVID-19 cases may expand more quickly in high HIV prevalence communities with poor health resources. The first reported cases of COVID-19 in South Africa occurred in early March from travelers who returned from Italy. South Africa has since reported over 400 cases (as of this writing), and the number continues to grow each day. Given the rapid spread of SARS-CoV-2 in South Africa, it now seems likely that COVID-19 cases will occur in all sub-Saharan African countries (Fig. 1 ). Perhaps what may be less certain is how SARS-CoV-2 will spread in HIV-endemic settings, and whether COVID-19 will have a higher morbidity and mortality rate among people living with HIV (PLHIV). In South Africa, where only 54% of the estimated 7.7 million PLHIV are virally suppressed and tuberculosis remains the leading cause of HIV-related mortality, these questions will need to be addressed. Fig. 1 Reported cases of COVID-19, as of March 24, 2020. (Source: World Health Organization [10]). Fig. 1 So far, little is known about the pathogenesis and clinical outcomes of COVID-19 in PLHIV. In this EClinicalMedicine issue, Dr. Zhao and colleagues describe a 50-year-old Chinese male living with HIV who had evidence of viral shedding for 39 days after symptom onset, but recovered after receiving human immunoglobulin, methylprednisolone, and inhaled interferon alpha-2b [4]. Another case report described a 61‐year‐old Chinese male with a history of diabetes, who presented with acute respiratory symptoms, and was newly diagnosed with both HIV and COVID-19 pneumonia [5]. The patient recovered after receiving steroid therapy, respiratory support, and starting antiretroviral therapy (ART). This author (PKD), however, had a 66-year-old American male with suppressed HIV recently succumb to COVID-19 pneumonia, despite ventilatory support and hydroxychloroquine. Currently, the US Centers for Disease Control and Prevention and the International AIDS Society consider PLHIV with low CD4+ T-cell count or not on ART as potentially vulnerable to more severe COVID-19 disease [6]. This concern is based on data from other respiratory diseases, including pneumococcal pneumonia and pulmonary tuberculosis, where PLHIV with compromised immunity have significantly worse health outcomes [7,8]. However, the experience from prior coronavirus outbreaks, including SARS CoV-1 and MERS, were limited among PLHIV, suggesting that PLHIV may not have a significantly higher risk of infection or mortality from SARS-CoV-2. For several years, the World Health Organization (WHO) has recommended a “Test and Treat” strategy to identify all PLHIV and initiate ART. The current treatment options for COVID-19 are limited and may not be effective—a randomized trial of lopinavir/ritonavir, a common HIV medication, had no clinical benefit, while clinical trials of hydroxychloroquine, Remdesivir, and Tocilizumab are ongoing [9]. With no proven therapeutic options for COVID-19, the WHO recommends a “Test, Test, Test” strategy in response to the SARS CoV-2 pandemic. Since the response to the HIV/AIDS epidemic was developed and refined over decades, some lessons may be applicable for the response to SARS CoV-2. First, establishing access to rapid, point-of-care COVID-19 testing in both community-based and clinical settings will be essential. The WHO has identified the development and evaluation of “rapid point-of-care diagnostics for use at the community level” as a top research priority [10]. Second, the mortality rate of HIV-associated TB has declined in part by initiating more PLHIV on ART. Starting ART may improve the immune response to COVID-19 for PLHIV, and may help prevent onset of Cytokine Release Syndrome or progression to severe respiratory failure. Third, the HIV epidemic led to crowded and overburdened health care facilities and hospitals. There is now a similar concern that COVID-19 will severely divert limited health care resources, which could reverse observed reductions in HIV and TB mortality in recent years. The public health response may need to incorporate additional COVID-specific resources, while still maintaining the supply chain of care and ART for PLHIV. With millions of PLHIV receiving ART throughout sub-Saharan Africa, perhaps the best way to protect this population from COVID-19 may be to ensure an uninterrupted supply of ART. As the COVID-19 response gathers momentum across sub-Saharan Africa, additional research will be needed to fully understand the susceptibility, transmission dynamics, pathogenesis and clinical outcomes of COVID-19 among PLHIV compared to the general population. Those most vulnerable to COVID-19 may be PLHIV who are either unaware of their diagnosis or not yet receiving ART. An important part of the response therefore will be not suspending the HIV 90-90-90 efforts during the SARS CoV-2 pandemic, but to expand ART in order to protect PLHIV from severe COVID-19 disease. Since the response will require adequate health care infrastructure, integrating COVID-19 testing services within the HIV treatment infrastructure may be essential for controlling the spread of SARS-CoV-2 in sub-Saharan Africa. Declaration of Competing Interest Dr. Paul K Drain reports receiving consulting or speaking fees from Gilead Science and Cepheid, and research support from the NIH, CDC, Gilead Sciences, and the Bill and Melinda Gates Foundation. He declares that he has no competing interests.

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          Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China

          Summary Background A recent cluster of pneumonia cases in Wuhan, China, was caused by a novel betacoronavirus, the 2019 novel coronavirus (2019-nCoV). We report the epidemiological, clinical, laboratory, and radiological characteristics and treatment and clinical outcomes of these patients. Methods All patients with suspected 2019-nCoV were admitted to a designated hospital in Wuhan. We prospectively collected and analysed data on patients with laboratory-confirmed 2019-nCoV infection by real-time RT-PCR and next-generation sequencing. Data were obtained with standardised data collection forms shared by WHO and the International Severe Acute Respiratory and Emerging Infection Consortium from electronic medical records. Researchers also directly communicated with patients or their families to ascertain epidemiological and symptom data. Outcomes were also compared between patients who had been admitted to the intensive care unit (ICU) and those who had not. Findings By Jan 2, 2020, 41 admitted hospital patients had been identified as having laboratory-confirmed 2019-nCoV infection. Most of the infected patients were men (30 [73%] of 41); less than half had underlying diseases (13 [32%]), including diabetes (eight [20%]), hypertension (six [15%]), and cardiovascular disease (six [15%]). Median age was 49·0 years (IQR 41·0–58·0). 27 (66%) of 41 patients had been exposed to Huanan seafood market. One family cluster was found. Common symptoms at onset of illness were fever (40 [98%] of 41 patients), cough (31 [76%]), and myalgia or fatigue (18 [44%]); less common symptoms were sputum production (11 [28%] of 39), headache (three [8%] of 38), haemoptysis (two [5%] of 39), and diarrhoea (one [3%] of 38). Dyspnoea developed in 22 (55%) of 40 patients (median time from illness onset to dyspnoea 8·0 days [IQR 5·0–13·0]). 26 (63%) of 41 patients had lymphopenia. All 41 patients had pneumonia with abnormal findings on chest CT. Complications included acute respiratory distress syndrome (12 [29%]), RNAaemia (six [15%]), acute cardiac injury (five [12%]) and secondary infection (four [10%]). 13 (32%) patients were admitted to an ICU and six (15%) died. Compared with non-ICU patients, ICU patients had higher plasma levels of IL2, IL7, IL10, GSCF, IP10, MCP1, MIP1A, and TNFα. Interpretation The 2019-nCoV infection caused clusters of severe respiratory illness similar to severe acute respiratory syndrome coronavirus and was associated with ICU admission and high mortality. Major gaps in our knowledge of the origin, epidemiology, duration of human transmission, and clinical spectrum of disease need fulfilment by future studies. Funding Ministry of Science and Technology, Chinese Academy of Medical Sciences, National Natural Science Foundation of China, and Beijing Municipal Science and Technology Commission.
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            Clinical Characteristics of 138 Hospitalized Patients With 2019 Novel Coronavirus–Infected Pneumonia in Wuhan, China

            In December 2019, novel coronavirus (2019-nCoV)-infected pneumonia (NCIP) occurred in Wuhan, China. The number of cases has increased rapidly but information on the clinical characteristics of affected patients is limited.
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              Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: a descriptive study

              Summary Background In December, 2019, a pneumonia associated with the 2019 novel coronavirus (2019-nCoV) emerged in Wuhan, China. We aimed to further clarify the epidemiological and clinical characteristics of 2019-nCoV pneumonia. Methods In this retrospective, single-centre study, we included all confirmed cases of 2019-nCoV in Wuhan Jinyintan Hospital from Jan 1 to Jan 20, 2020. Cases were confirmed by real-time RT-PCR and were analysed for epidemiological, demographic, clinical, and radiological features and laboratory data. Outcomes were followed up until Jan 25, 2020. Findings Of the 99 patients with 2019-nCoV pneumonia, 49 (49%) had a history of exposure to the Huanan seafood market. The average age of the patients was 55·5 years (SD 13·1), including 67 men and 32 women. 2019-nCoV was detected in all patients by real-time RT-PCR. 50 (51%) patients had chronic diseases. Patients had clinical manifestations of fever (82 [83%] patients), cough (81 [82%] patients), shortness of breath (31 [31%] patients), muscle ache (11 [11%] patients), confusion (nine [9%] patients), headache (eight [8%] patients), sore throat (five [5%] patients), rhinorrhoea (four [4%] patients), chest pain (two [2%] patients), diarrhoea (two [2%] patients), and nausea and vomiting (one [1%] patient). According to imaging examination, 74 (75%) patients showed bilateral pneumonia, 14 (14%) patients showed multiple mottling and ground-glass opacity, and one (1%) patient had pneumothorax. 17 (17%) patients developed acute respiratory distress syndrome and, among them, 11 (11%) patients worsened in a short period of time and died of multiple organ failure. Interpretation The 2019-nCoV infection was of clustering onset, is more likely to affect older males with comorbidities, and can result in severe and even fatal respiratory diseases such as acute respiratory distress syndrome. In general, characteristics of patients who died were in line with the MuLBSTA score, an early warning model for predicting mortality in viral pneumonia. Further investigation is needed to explore the applicability of the MuLBSTA score in predicting the risk of mortality in 2019-nCoV infection. Funding National Key R&D Program of China.
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                Author and article information

                Contributors
                Journal
                EClinicalMedicine
                EClinicalMedicine
                EClinicalMedicine
                The Author(s). Published by Elsevier Ltd.
                2589-5370
                22 April 2020
                22 April 2020
                : 100342
                Affiliations
                [a ]Department of Global Health, Schools of Medicine and Public Health, University of Washington, Seattle, WA, USA
                [b ]Department of Medicine, School of Medicine, University of Washington, Seattle, USA
                [c ]Department of Epidemiology, School of Public Health, University of Washington, Seattle, USA
                [d ]Centre for the AIDS Programme of Research in South Africa (CAPRISA), University of KwaZulu–Natal, Durban, South Africa
                [e ]Discipline of Public Health Medicine, School of Nursing and Public Health, University of KwaZulu-Natal, Durban, South Africa
                Author notes
                [* ]Corresponding author at: Department of Global Health, Schools of Medicine and Public Health, University of Washington, 325 Ninth Ave, UW Box 359927, Seattle, WA 98104-2420, USA. pkdrain@ 123456uw.edu
                Article
                S2589-5370(20)30086-9 100342
                10.1016/j.eclinm.2020.100342
                7174187
                4f37c6ce-4346-4847-8338-0ed11decf071
                © 2020 The Author(s)

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

                History
                : 26 March 2020
                : 26 March 2020
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