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1.
J Leukoc Biol ; 112(1): 201-212, 2022 07.
Artículo en Inglés | MEDLINE | ID: covidwho-2075041

RESUMEN

T cells are thought to be an important correlates of protection against SARS-CoV2 infection. However, the composition of T cell subsets in convalescent individuals of SARS-CoV2 infection has not been well studied. The authors determined the lymphocyte absolute counts, the frequency of memory T cell subsets, and the plasma levels of common γ-chain in 7 groups of COVID-19 individuals, based on days since RT-PCR confirmation of SARS-CoV-2 infection. The data show that both absolute counts and frequencies of lymphocytes as well as, the frequencies of CD4+ central and effector memory cells increased, and the frequencies of CD4+ naïve T cells, transitional memory, stem cell memory T cells, and regulatory cells decreased from Days 15-30 to Days 61-90 and plateaued thereafter. In addition, the frequencies of CD8+ central memory, effector, and terminal effector memory T cells increased, and the frequencies of CD8+ naïve cells, transitional memory, and stem cell memory T cells decreased from Days 15-30 to Days 61-90 and plateaued thereafter. The plasma levels of IL-2, IL-7, IL-15, and IL-21-common γc cytokines started decreasing from Days 15-30 till Days 151-180. Severe COVID-19 patients exhibit decreased levels of lymphocyte counts and frequencies, higher frequencies of naïve cells, regulatory T cells, lower frequencies of central memory, effector memory, and stem cell memory, and elevated plasma levels of IL-2, IL-7, IL-15, and IL-21. Finally, there was a significant correlation between memory T cell subsets and common γc cytokines. Thus, the study provides evidence of alterations in lymphocyte counts, memory T cell subset frequencies, and common γ-chain cytokines in convalescent COVID-19 individuals.


Asunto(s)
COVID-19 , Citocinas , Células T de Memoria , Linfocitos T CD4-Positivos , Linfocitos T CD8-positivos , COVID-19/sangre , COVID-19/inmunología , Convalecencia , Citocinas/sangre , Humanos , Memoria Inmunológica/inmunología , Interleucina-15/sangre , Interleucina-2/sangre , Interleucina-7/sangre , Células T de Memoria/inmunología , ARN Viral , SARS-CoV-2 , Subgrupos de Linfocitos T/inmunología
2.
researchsquare; 2022.
Preprint en Inglés | PREPRINT-RESEARCHSQUARE | ID: ppzbmed-10.21203.rs.3.rs-2048496.v1

RESUMEN

Background The Coronavirus disease 2019 (COVID-19) pandemic increased the utilisation of healthcare services. Such utilization could lead to higher out-of-pocket expenditure (OOPE) and catastrophic health expenditures (CHE). We estimated OOPE and the proportion of households that experienced CHE by conducting a cross-sectional survey of 1200 randomly selected COVID-19.Methods A cross-sectional survey was conducted by telephonic interviews of 1200 randomly selected COVID-19 patients who tested positive between 1 March and 31 August 2021. We collected household-level information on demographics, income, expenditure, insurance coverage, direct medical and non-medical costs incurred toward COVID-19 management. We estimated the proportion of CHE with a 95% Confidence interval. Multivariate logistic regression was used to examine the association between the number of severe COVID-19 and CHE.Results The mean OOPE per household was INR 122,221 (92,744 to 51,698) [US$1,643 (1,247 to 2,040)]. Among households, 61.7% faced OOPE, and 25.8% experienced CHE due to COVID-19. The odds of facing CHE were high among the households; with a family member over 65 years [OR = 2.89 (2.03 to 4.12)], with a comorbid individual [OR = 3.38 (2.41 to 4.75)], in the lowest income quintile [OR = 1.82 (1.12 to 2.95)], any member visited private hospital [OR = 11.85 (7.68 to 18.27)]. The odds of having CHE in a household who have received insurance claims [OR = 5.8 (2.81 to 11.97)] were high. Households having one severe COVID-19 and more than one increased the risk of CHE by four-times [AOR = 4.33 (2.13–8.34)] and five-times [AOR = 5.10 (2.42–10.74)] respectively.Conclusion COVID-19 severity increases household OOPE and CHE. Strengthening the public healthcare and health insurance with higher health financing is indispensable for financial risk protection of households with severe COVID-19 from CHE.


Asunto(s)
COVID-19
3.
Viruses ; 14(3)2022 03 02.
Artículo en Inglés | MEDLINE | ID: covidwho-1715786

RESUMEN

BACKGROUND: Examination of CD4+ T cell responses during the natural course of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection offers useful information for the improvement of vaccination strategies against this virus and the protective effect of these T cells. METHODS: We characterized the SARS-CoV-2-specific CD4+ T cell activation marker, multifunctional cytokine and cytotoxic marker expression in recovered coronavirus disease 2019 (COVID-19) individuals. RESULTS: CD4+ T-cell responses in late convalescent (>6 months of diagnosis) individuals are characterized by elevated frequencies of activated as well as mono, dual- and multi-functional Th1 and Th17 CD4+ T cells in comparison to early convalescent (<1 month of diagnosis) individuals following stimulation with SARS-CoV-2-specific antigens. Similarly, the frequencies of cytotoxic marker expressing CD4+ T cells were also enhanced in late convalescent compared to early convalescent individuals. CONCLUSION: Our findings from a low-to middle-income country suggest protective adaptive immune responses following natural infection of SARS-CoV-2 are elevated even at six months following initial symptoms, indicating the CD4+ T cell mediated immune protection lasts for six months or more in natural infection.


Asunto(s)
COVID-19 , Linfocitos T CD4-Positivos , Humanos , Inmunidad Humoral , Activación de Linfocitos , SARS-CoV-2
4.
BMJ Open ; 11(11): e051491, 2021 11 05.
Artículo en Inglés | MEDLINE | ID: covidwho-1504156

RESUMEN

OBJECTIVE: To describe the characteristics of contacts of patients with COVID-19 case in terms of time, place and person, to calculate the secondary attack rate (SAR) and factors associated with COVID-19 infection among contacts. DESIGN: A retrospective cohort study SETTING AND PARTICIPANTS: Contacts of cases identified by the health department from 14 March 2020to 30 May 2020, in 9 of 38 administrative districts of Tamil Nadu. Significant proportion of cases attended a religious congregation. OUTCOME MEASURE: Attack rate among the contacts and factors associated with COVID-19 positivity. RESULTS: We listed 15 702 contacts of 931 primary cases. Of the contacts, 89% (n: 14 002) were tested for COVID-19. The overall SAR was 4% (599/14 002), with higher among the household contacts (13%) than the community contacts (1%). SAR among the contacts of primary cases with congregation exposure were 5 times higher than the contacts of non-congregation primary cases (10% vs 2%). Being a household contact of a primary case with congregation exposure had a fourfold increased risk of getting COVID-19 (relative risk (RR): 16.4; 95% CI: 13 to 20) than contact of primary case without congregation exposure. Among the symptomatic primary cases, household contacts of congregation primaries had higher RR than household contacts of other cases ((RR: 25.3; 95% CI: 10.2 to 63) vs (RR: 14.6; 95% CI: 5.7 to 37.7)). Among asymptomatic primary case, RR was increased among household contacts (RR: 16.5; 95% CI: 13.2 to 20.7) of congregation primaries compared with others. CONCLUSION: Our study showed an increase in disease transmission among household contacts than community contacts. Also, symptomatic primary cases and primary cases with exposure to the congregation had more secondary cases than others.


Asunto(s)
COVID-19 , Trazado de Contacto , Humanos , Incidencia , India/epidemiología , Estudios Retrospectivos , Factores de Riesgo , SARS-CoV-2
5.
Manoj V. Murhekar; Tarun Bhatnagar; Jeromie Wesley Vivian Thangaraj; V. Saravanakumar; Muthusamy Santhosh Kumar; Sriram Selvaraju; Kirankumar Rade; C.P. Girish Kumar; R. Sabarinathan; Alka Turuk; Nivethitha N. Krishnan; Aby Robinson; Nivetha Srinivasan; Smita Asthana; Rakesh Balachandar; Sampada Dipak Bangar; Avi Kumar Bansal; Jyothi Bhat; Vishal Chopra; Dasarathi Das; Alok Kumar Deb; Kangjam Rekha Devi; Gaurav Raj Dwivedi; S. Muhammad Salim Khan; M. Sunil Kumar; Avula Laxmaiah; Major Madhukar; Amarendra Mahapatra; Chethana Rangaraju; Jyotirmayee Turuk; Suresh Yadav; P. K. Anand; Rushikesh Andhalkar; Nimmathota Arlappa; Khalid Bashir; Dinesh Kumar Baradwaj; Pravin Bharti; Debdutta Bhattacharya; Sthita Pragnya Behera; Ashrafjit S. Chahal; Debjit Chakraborty; Anshuman Chaudhury; Hirawati Deval; Sarang Dhatrak; Vikas Dhikav; Rakesh Dayal; Prathiksha Giridharan; Inaamul Haq; Babu Jagjeevan; Agam Jain; Arshad Kalliath; Srikanta Kanungo; T. Karunakaran; Jaya Singh Kshatri; Niraj Kumar; Vijay Kumar; V.G. Vinod Kumar; Gangeti Gandhi Jayanthi Naga Lakshmi; Ganesh Mehta; Anindya Mitra; K. Nagbhushanam; A.R. Nirmala; Subrat Kumar Palo; Ashok Kumar Pandey; Ganta Venkata Prasad; Uday Kumar Pucha; Mariya Amin Qurieshi; Vikas Sabaharwal; Seema Sahay; Ramesh Kumar Sangwan; Rochak Saxena; Krithikaa Sekar; Vijay Kumar Shukla; Hari Bhan Singh; Prashant Kumar Singh; Pushpendra Singh; Rajeev Singh; Mahendra Thakor; Dantuluri Sheethal Varma; Ankit Viramgami; Pradeep A. Menon; Rajiv Yadav; Surabhi Yadav; Manjula Singh; Amit Chakrabarti; Aparup Das; Shanta Dutta; Rajni Kant; A.M. Khan; Kanwar Narain; Somashekar Narasimhaiah; Chandrasekaran Padmapriyadarshini; Krishna Pandey; Sanghamitra Pati; Hemalatha Rajkumar; T. Ramesh; Arun Kumar Sharma; Y.K. Sharma; Shalini Singh; Samiran Panda; D.C.S. Reddy; Balram Bhargava.
ssrn; 2021.
Preprint en Inglés | PREPRINT-SSRN | ID: ppzbmed-10.2139.ssrn.3899801
6.
Manoj V. Murhekar; Tarun Bhatnagar; Jeromie Wesley Vivian Thangaraj; V. Saravanakumar; Muthusamy Santhosh Kumar; Sriram Selvaraju; Kiran Rade; C.P. Girish Kumar; R. Sabarinathan; Alka Turuk; Smita Asthana; Rakesh Balachandar; Sampada Dipak Bangar; Avi Kumar Bansal; Vishal Chopra; Dasarathi Das; Alok Kumar Deb; Kangjam Rekha Devi; Vikas Dhikav; Gaurav Raj Dwivedi; S. Muhammad Salim Khan; M. Sunil Kumar; Avula Laxmaiah; Major Madhukar; Amarendra Mahapatra; Chethana Rangaraju; Jyotirmayee Turuk; Rajiv Yadav; Rushikesh Andhalkar; K. Arunraj; Dinesh Kumar Baradwaj; Pravin Bharti; Debdutta Bhattacharya; Jyothi Bhat; Ashrafjit S. Chahal; Debjit Chakraborty; Anshuman Chaudhury; Hirawati Deval; Sarang Dhatrak; Rakesh Dayal; D. Elantamilan; Prathiksha Giridharan; Inaamul Haq; Ramesh Kumar Hudda; Babu Jagjeevan; Arshad Kalliath; Srikanta Kanungo; Nivethitha N. Krishnan; Jaya Singh Kshatri; Alok Kumar; Niraj Kumar; V.G. Vinoth Kumar; Gangeti Gandhi Jayanthi Naga Lakshmi; Ganesh Mehta; Nandan Kumar Mishra; Anindya Mitra; K. Nagbhushanam; Arlappa Nimmathota; A.R. Nirmala; Ashok Kumar Pandey; Ganta Venkata Prasad; Mariya Amin Qurieshi; Sirasanambatti Devarajulu Reddy; Aby Robinson; Seema Sahay; Rochak Saxena; Krithikaa Sekar; Vijay Kumar Shukla; Hari Bhan Singh; Prashant Kumar Singh; Pushpendra Singh; Rajeev Singh; Nivetha Srinivasan; Dantuluri Sheethal Varma; Ankit Viramgami; Vimith Cheruvathoor Wilson; Surabhi Yadav; Suresh Yadav; Kamran Zaman; Amit Chakrabarti; Aparup Das; R.S. Dhaliwal; Shanta Dutta; Rajni Kant; A.M. Khan; Kanwar Narain; Somashekar Narasimhaiah; Chandrasekaran Padmapriyadarshini; Krishna Pandey; Sanghamitra Pati; Shripad Patil; Hemalatha Rajkumar; Tekumalla Ramarao; Y.K. Sharma; Shalini Singh; Samiran Panda; D.C.S. Reddy; Balram Bhargava.
ssrn; 2021.
Preprint en Inglés | PREPRINT-SSRN | ID: ppzbmed-10.2139.ssrn.3797589
7.
Manoj V. Murhekar; Tarun Bhatnagar; Jeromie Wesley Vivian Thangaraj; V. Saravanakumar; Muthusamy Santhosh Kumar; Sriram Selvaraju; Kiran Rade; Girish Kumar CP; R. Sabarinathan; Alka Turuk; Smita Asthana; Rakesh Balachandar; Sampada Dipak Bangar; Avi Kumar Bansal; Vishal Chopra; Dasarathi Das; Alok Kumar Deb; Kangjam Rekha Devi; Vikas Dhikav; Gaurav Raj Dwivedi; S. Muhammad Salim Khan; M. Sunil Kumar; Avula Laxmaiah; Major Madhukar; Amarendra Mahapatra; Chethana Rangaraju; Jyotirmayee Turuk; Rajiv Yadav; Rushikesh Andhalkar; K. Arunraj; Dinesh Kumar Baradwaj; Pravin Bharti; Debdutta Bhattacharya; Jyothi Bhat; Ashrafjit S. Chahal; Debjit Chakraborty; Anshuman Chaudhury; Hirawati Deval; Sarang Dhatrak; Rakesh Dayal; D. Elantamilan; Prathiksha Giridharan; Inaamul Haq; Ramesh Kumar Hudda; Babu Jagjeevan; Arshad Kalliath; Srikanta Kanungo; Nivethitha N. Krishnan; Jaya Singh Kshatri; Alok Kumar; Niraj Kumar; V.G. Vinoth Kumar; Gangeti Gandhi Jayanthi Naga Lakshmi; Ganesh Mehta; Nandan Kumar Mishra; Anindya Mitra; K. Nagbhushanam; Arlappa Nimmathota; A.R. Nirmala; Ashok Kumar Pandey; Ganta Venkata Prasad; Mariya Amin Qurieshi; Sirasanambatti Devarajulu Reddy; Aby Robinson; Seema Sahay; Rochak Saxena; Krithikaa Sekar; Vijay Kumar Shukla; Hari Bhan Singh; Prashant Kumar Singh; Pushpendra Singh; Rajeev Singh; Nivetha Srinivasan; Dantuluri Sheethal Varma; Ankit Viramgami; Vimith Cheruvathoor Wilson; Surabhi Yadav; Suresh Yadav; Kamran Zaman; Amit Chakrabarti; Aparup Das; R.S. Dhaliwal; Shanta Dutta; Rajni Kant; A M Khan; Kanwar Narain; Somashekar Narasimhaiah; Chandrasekaran Padmapriyadarshini; Krishna Pandey; Sanghamitra Pati; Shripad Patil; Hemalatha Rajkumar; Tekumalla Ramarao; Y.K. Sharma; Shalini Singh; Samiran Panda; D.C.S. Reddy; Balram Bhargava; ICMR Serosurveillance Group.
ssrn; 2021.
Preprint en Inglés | PREPRINT-SSRN | ID: ppzbmed-10.2139.ssrn.3810375
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