Immunogenicity, Effectiveness, and Safety of COVID-19 Vaccines among Patients with Immune-Mediated Dermatological Diseases: A Systematic Review and Meta-analysis

Authors

  • Sonphet Chirasuthat Division of Dermatology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand https://orcid.org/0009-0001-2477-9149
  • Yanisa Ratanapokasatit Division of Dermatology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand https://orcid.org/0000-0001-8303-3323
  • Kunlawat Thadanipon 1Division of Dermatology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand; Department of Clinical Epidemiology and Biostatistics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand https://orcid.org/0000-0001-6324-2312
  • Kumutnart Chanprapaph Division of Dermatology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand https://orcid.org/0000-0001-7931-3816

DOI:

https://doi.org/10.2340/actadv.v104.40009

Keywords:

COVID-19 Vaccines, Immune System Diseases, Immunosuppression Therapy, Meta-Analysis, Skin Diseases

Abstract

Immunocompromised individuals, primarily attributable to using immunosuppressants, face heightened COVID-19 risks. Despite the proven efficacy of COVID-19 vaccines, their impact on patients with immune-mediated dermatological diseases remains unclear. This study aims to thoroughly examine vaccine immunogenicity, effectiveness, and safety in immune-mediated dermatological disease patients. Clinical studies in adults that compared vaccinated immune-mediated dermatological disease patients with vaccinated healthy controls or unvaccinated immune-mediated dermatological disease patients in terms of vaccine immunogenicity, COVID-19 infection, adverse events, or exacerbation of immune-mediated dermatological diseases were searched via electronic databases. Seventeen studies (1,348,690 participants) were included. Seroconversion rates between immune-mediated dermatological disease patients and healthy controls were not different. However, among individuals aged ≤55 years, immune-mediated dermatological disease patients had lower mean anti-SARS-CoV-2 IgG levels. Immunosuppressed immune-mediated dermatological disease patients also had lower titres and were less likely to achieve T-cell response. In terms of safety, the risk of adverse events was higher in atopic dermatitis patients, but those with psoriasis had a reduced risk. Additionally, immunosuppressed patients had fewer adverse events. Vaccinated immune-mediated dermatological disease patients had a lower risk of COVID-19 infection than unvaccinated patients but a higher risk than healthy controls; however, disease exacerbation may be induced. In conclusion, immune-mediated dermatological diseases showed a reduced vaccine response in our meta-analysis, yet vaccination remained effective against COVID-19 infection and well tolerated.

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References

Pormohammad A, Zarei M, Ghorbani S, Mohammadi M, Razizadeh MH, Turner DL, et al. Efficacy and safety of COVID-19 vaccines: a systematic review and meta-analysis of randomized clinical trials. Vaccines 2021; 9: 467.

https://doi.org/10.3390/vaccines9050467 DOI: https://doi.org/10.3390/vaccines9050467

Sharif N, Alzahrani KJ, Ahmed SN, Dey SK. Efficacy, immunogenicity and safety of COVID-19 vaccines: a systematic review and meta-analysis. Front Immunol 2021; 12: 714170.

https://doi.org/10.3389/fimmu.2021.714170 DOI: https://doi.org/10.3389/fimmu.2021.714170

Liu Q, Qin C, Liu M, Liu J. Effectiveness and safety of SARS-CoV-2 vaccine in real-world studies: a systematic review and meta-analysis. Infect Dis Poverty 2021; 10: 132.

https://doi.org/10.1186/s40249-021-00915-3 DOI: https://doi.org/10.1186/s40249-021-00915-3

Zeng B, Gao L, Zhou Q, Yu K, Sun F. Effectiveness of COVID-19 vaccines against SARS-CoV-2 variants of concern: a systematic review and meta-analysis. BMC Med 2022; 20: 200.

https://doi.org/10.1186/s12916-022-02397-y DOI: https://doi.org/10.1186/s12916-022-02397-y

Rotshild V, Hirsh-Raccah B, Miskin I, Muszkat M, Matok I. Comparing the clinical efficacy of COVID-19 vaccines: a systematic review and network meta-analysis. Sci Rep 2021; 11: 22777.

https://doi.org/10.1038/s41598-021-02321-z DOI: https://doi.org/10.1038/s41598-021-02321-z

Wu Q, Dudley MZ, Chen X, Bai X, Dong K, Zhuang T, et al. Evaluation of the safety profile of COVID-19 vaccines: a rapid review. BMC Med 2021; 19: 173.

https://doi.org/10.1186/s12916-021-02059-5 DOI: https://doi.org/10.1186/s12916-021-02059-5

Manuel O, Estabrook M. RNA respiratory viral infections in solid organ transplant recipients: guidelines from the American Society of Transplantation Infectious Diseases Community of Practice. Clin Transplant 2019; 33: e13511.

https://doi.org/10.1111/ctr.13511 DOI: https://doi.org/10.1111/ctr.13511

Couch RB, Englund JA, Whimbey E. Respiratory viral infections in immunocompetent and immunocompromised persons. Am J Med 1997; 102: 2-9.

https://doi.org/10.1016/S0002-9343(97)00003-X DOI: https://doi.org/10.1016/S0002-9343(97)00003-X

Coronavirus Disease 2019 (COVID-19) Treatment guidelines. Bethesda (MD): National Institutes of Health (US); 2021.

Jayasinghe S, Patel C, Armstrong L, Chiu C, Macartney K, Flanagan K, et al. ATAGI Targeted Review 2021: the national COVID-19 vaccination program. Commun Dis Intell (2018) 2023; 47.

https://doi.org/10.33321/cdi.2023.47.20 DOI: https://doi.org/10.33321/cdi.2023.47.20

Shoham S, Batista C, Ben Amor Y, Ergonul O, Hassanain M, Hotez P, et al. Vaccines and therapeutics for immunocompromised patients with COVID-19. EClinicalMedicine 2023; 59: 101965.

https://doi.org/10.1016/j.eclinm.2023.101965 DOI: https://doi.org/10.1016/j.eclinm.2023.101965

Sakuraba A, Luna A, Micic D. Serologic response to coronavirus disease 2019 (COVID-19) vaccination in patients with immune-mediated inflammatory diseases: a systematic review and meta-analysis. Gastroenterology 2022; 162: 88-108.

https://doi.org/10.1053/j.gastro.2021.09.055 DOI: https://doi.org/10.1053/j.gastro.2021.09.055

Lee ARYB, Wong SY, Tay SH. Booster COVID-19 vaccines for immune-mediated inflammatory disease patients: a systematic review and meta-analysis of efficacy and safety. Vaccines 2022; 10: 668.

https://doi.org/10.3390/vaccines10050668 DOI: https://doi.org/10.3390/vaccines10050668

Sakuraba A, Luna A, Micic D. A systematic review and meta-analysis of serologic response following coronavirus disease 2019 (COVID-19) vaccination in solid organ transplant recipients. Viruses 2022; 14: 1822.

https://doi.org/10.3390/v14081822 DOI: https://doi.org/10.3390/v14081822

Sood A, Tran M, Murthy V, Gonzalez E. Immunogenicity and safety of SARS-CoV-2 vaccination in patients with rheumatic diseases: a systematic review and meta-analysis. J Clin Rheumatol 2022; 28: 381-389.

https://doi.org/10.1097/RHU.0000000000001871 DOI: https://doi.org/10.1097/RHU.0000000000001871

Sung KY, Chang TE, Wang YP, Lin CC, Chang CY, Hou MC, et al. SARS-CoV-2 vaccination in patients with inflammatory bowel disease: a systemic review and meta-analysis. J Chin Med Assoc 2022; 85: 421-430.

https://doi.org/10.1097/JCMA.0000000000000682 DOI: https://doi.org/10.1097/JCMA.0000000000000682

Bhurwal A, Mutneja H, Bansal V, Goel A, Arora S, Attar B, et al. Effectiveness and safety of SARS-CoV-2 vaccine in inflammatory bowel disease patients: a systematic review, meta-analysis and meta-regression. Aliment Pharmacol Ther 2022; 55: 1244-1264.

https://doi.org/10.1111/apt.16913 DOI: https://doi.org/10.1111/apt.16913

James D, Jena A, Bharath PN, Choudhury A, Singh AK, Sebastian S, et al. Safety of SARS-CoV-2 vaccination in patients with inflammatory bowel disease: a systematic review and meta-analysis. Dig Liver Dis 2022; 54: 713-721.

https://doi.org/10.1016/j.dld.2022.03.005 DOI: https://doi.org/10.1016/j.dld.2022.03.005

Page MJ, McKenzie JE, Bossuyt PM, Boutron I, Hoffmann TC, Mulrow CD, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ 2021; 372: 71.

https://doi.org/10.1136/bmj.n71 DOI: https://doi.org/10.1136/bmj.n71

Stang A. Critical evaluation of the Newcastle-Ottawa scale for the assessment of the quality of nonrandomized studies in meta-analyses. Eur J Epidemiol 2010; 25: 603-605.

https://doi.org/10.1007/s10654-010-9491-z DOI: https://doi.org/10.1007/s10654-010-9491-z

Sterne JA, Hernán MA, Reeves BC, Savović J, Berkman ND, Viswanathan M, et al. ROBINS-I: a tool for assessing risk of bias in non-randomised studies of interventions. BMJ 2016; 355: i4919.

https://doi.org/10.1136/bmj.i4919 DOI: https://doi.org/10.1136/bmj.i4919

Wan X, Wang W, Liu J, Tong T. Estimating the sample mean and standard deviation from the sample size, median, range and/or interquartile range. BMC Med Res Methodol 2014; 14: 135.

https://doi.org/10.1186/1471-2288-14-135 DOI: https://doi.org/10.1186/1471-2288-14-135

Kristiansen PA, Page M, Bernasconi V, Mattiuzzo G, Dull P, Makar K, et al. WHO International Standard for anti-SARS-CoV-2 immunoglobulin. Lancet 2021; 397: 1347-1348.

https://doi.org/10.1016/S0140-6736(21)00527-4 DOI: https://doi.org/10.1016/S0140-6736(21)00527-4

Graceffa D, Sperati F, Bonifati C, Spoletini G, Lora V, Pimpinelli F, et al. Immunogenicity of three doses of anti-SARS-CoV-2 BNT162b2 vaccine in psoriasis patients treated with biologics. Front Med 2022; 9: 961904.

https://doi.org/10.3389/fmed.2022.961904 DOI: https://doi.org/10.3389/fmed.2022.961904

Kridin K, Schonmann Y, Onn E, Bitan DT, Weinstein O, Cohen AD. Determinants and effectiveness of BNT162b2 mRNA vaccination among patients with atopic dermatitis: a population-based study. Am J Clin Dermatol 2022; 23: 385-392.

https://doi.org/10.1007/s40257-022-00672-5 DOI: https://doi.org/10.1007/s40257-022-00672-5

Özgen Z, Aksoy H, Akın Çakıcı Ö, Koku Aksu AE, Erdem O, Kara Polat A, et al. COVID-19 severity and SARS-Cov-2 vaccine safety in pemphigus patients. Dermatol Ther 2022; 35: e15417.

https://doi.org/10.1111/dth.15417 DOI: https://doi.org/10.1111/dth.15417

Mahil SK, Bechman K, Raharja A, Domingo-Vila C, Baudry D, Brown MA, et al. Humoral and cellular immunogenicity to a second dose of COVID-19 vaccine BNT162b2 in people receiving methotrexate or targeted immunosuppression: a longitudinal cohort study. Lancet Rheumatol 2022; 4: 42-52.

https://doi.org/10.1016/S2665-9913(21)00333-7 DOI: https://doi.org/10.1016/S2665-9913(21)00333-7

Mahil SK, Bechman K, Raharja A, Domingo-Vila C, Baudry D, Brown MA, et al. The effect of methotrexate and targeted immunosuppression on humoral and cellular immune responses to the COVID-19 vaccine BNT162b2: a cohort study. Lancet Rheumatol 2021; 3: 627-637.

https://doi.org/10.1016/S2665-9913(21)00212-5 DOI: https://doi.org/10.1016/S2665-9913(21)00212-5

Pakhchanian H, Raiker R, Wolf M, Trotter SC. Examining the risk of breakthrough infection and COVID-19 vaccination safety in patients with atopic dermatitis. Br J Dermatol 2022; 187: 251-253.

https://doi.org/10.1111/bjd.21038 DOI: https://doi.org/10.1111/bjd.21038

Huang YW, Tsai TF. Exacerbation of psoriasis following COVID-19 vaccination: report from a single center. Front Med 2021; 8: 812010.

https://doi.org/10.3389/fmed.2021.812010 DOI: https://doi.org/10.3389/fmed.2021.812010

Koç Yıldırım S, Demirel Öğüt N, Erbağcı E. Retrospective evaluation of patients with chronic spontaneous urticaria using omalizumab during the COVID-19 pandemic. J Cosmet Dermatol 2022; 21: 431-434.

https://doi.org/10.1111/jocd.14725 DOI: https://doi.org/10.1111/jocd.14725

Chanprapaph K, Seree-Aphinan C, Rattanakaemakorn P, Pomsoong C, Ratanapokasatit Y, Setthaudom C, et al. A real-world prospective cohort study of immunogenicity and reactogenicity of ChAdOx1-S[recombinant] among patients with immune-mediated dermatologic diseases. Br J Dermatol 2023; 188: 268-277.

https://doi.org/10.1093/bjd/ljac045 DOI: https://doi.org/10.1093/bjd/ljac045

Cristaudo A, Graceffa D, Pimpinelli F, Sperati F, Spoletini G, Bonifati C, et al. Immunogenicity and safety of anti-SARS-CoV-2 BNT162b2 vaccine in psoriasis patients treated with biologic drugs. J Eur Acad Dermatol Venereol 2022; 36: 266-268.

https://doi.org/10.1111/jdv.17861 DOI: https://doi.org/10.1111/jdv.17861

Piros ÉA, Cseprekál O, Görög A, Hidvégi B, Medvecz M, Szabó Z, et al. Seroconversion after anti-SARS-CoV-2 mRNA vaccinations among moderate-to-severe psoriatic patients receiving systemic biologicals: prospective observational cohort study. Dermatol Ther 2022; 35: e15408.

https://doi.org/10.1111/dth.15408

Pavlotsky F, Segal Z, Barzilai A. Antibody response to BNT162b2 vaccine in immune modifiers-treated psoriatic patients. J Psoriasis Psoriatic Arthritis 2022; 7: 24-28.

https://doi.org/10.1177/24755303211056059 DOI: https://doi.org/10.1177/24755303211056059

Seree-Aphinan C, Chanprapaph K, Rattanakaemakorn P, Setthaudom C, Suangtamai T, Pomsoong C, et al. Inactivated COVID-19 vaccine induces a low humoral immune response in a subset of dermatological patients receiving immunosuppressants. Front Med 2021; 8: 769845.

https://doi.org/10.3389/fmed.2021.769845 DOI: https://doi.org/10.3389/fmed.2021.769845

Megna M, Potestio L, Battista T, Camela E, Genco L, Noto M, et al. Immune response to COVID-19 mRNA vaccination in patients with psoriasis undergoing treatment with biologics. Clin Exp Dermatol 2022; 47: 2310-2312.

https://doi.org/10.1111/ced.15395 DOI: https://doi.org/10.1111/ced.15395

Jena A, Mishra S, Deepak P, Kumar MP, Sharma A, Patel YI, et al. Response to SARS-CoV-2 vaccination in immune mediated inflammatory diseases: systematic review and meta-analysis. Autoimmun Rev 2022; 21: 102927.

https://doi.org/10.1016/j.autrev.2021.102927 DOI: https://doi.org/10.1016/j.autrev.2021.102927

Jena A, James D, Singh AK, Dutta U, Sebastian S, Sharma V. Effectiveness and durability of COVID-19 vaccination in 9447 patients with IBD: a systematic review and meta-analysis. Clin Gastroenterol Hepatol 2022; 20: 1456-1479.

https://doi.org/10.1016/j.cgh.2022.02.030 DOI: https://doi.org/10.1016/j.cgh.2022.02.030

Sakuraba A, Luna A, Micic D. Serologic response following SARS-COV2 vaccination in patients with cancer: a systematic review and meta-analysis. J Hematol Oncol 2022; 15: 15.

https://doi.org/10.1186/s13045-022-01233-3 DOI: https://doi.org/10.1186/s13045-022-01233-3

Seyahi E, Bakhdiyarli G, Oztas M, Kuskucu MA, Tok Y, Sut N, et al. Antibody response to inactivated COVID-19 vaccine (CoronaVac) in immune-mediated diseases: a controlled study among hospital workers and elderly. Rheumatol Int 2021; 41: 1429-1440.

https://doi.org/10.1007/s00296-021-04910-7 DOI: https://doi.org/10.1007/s00296-021-04910-7

Kostianovsky A, Charles P, Alves JF, Goulet M, Pagnoux C, Le Guern V, et al. Immunogenicity and safety of seasonal and 2009 pandemic A/H1N1 influenza vaccines for patients with autoimmune diseases: a prospective, monocentre trial on 199 patients. Clin Exp Rheumatol 2012; 30: S83-S89.

Elkayam O, Yaron M, Caspi D. Safety and efficacy of vaccination against hepatitis B in patients with rheumatoid arthritis. Ann Rheum Dis 2002; 61: 623-625.

https://doi.org/10.1136/ard.61.7.623 DOI: https://doi.org/10.1136/ard.61.7.623

Erkek E, Ayaslioglu E, Erkek AB, Kurtipek GS, Bagci Y. Response to vaccination against hepatitis B in patients with Behcet's disease. J Gastroenterol Hepatol 2005; 20: 1508-1511.

https://doi.org/10.1111/j.1440-1746.2005.03903.x DOI: https://doi.org/10.1111/j.1440-1746.2005.03903.x

McMahan ZH, Bingham CO 3rd. Effects of biological and non-biological immunomodulatory therapies on the immunogenicity of vaccines in patients with rheumatic diseases. Arthritis Res Ther 2014; 16: 506.

https://doi.org/10.1186/s13075-014-0506-0 DOI: https://doi.org/10.1186/s13075-014-0506-0

Bingham CO 3rd, Looney RJ, Deodhar A, Halsey N, Greenwald M, Codding C, et al. Immunization responses in rheumatoid arthritis patients treated with rituximab: results from a controlled clinical trial. Arthritis Rheum 2010; 62: 64-74.

https://doi.org/10.1002/art.25034 DOI: https://doi.org/10.1002/art.25034

Crooke SN, Ovsyannikova IG, Poland GA, Kennedy RB. Immunosenescence and human vaccine immune responses. Immun Ageing 2019; 16: 25.

https://doi.org/10.1186/s12979-019-0164-9 DOI: https://doi.org/10.1186/s12979-019-0164-9

Stiasny K, Aberle JH, Keller M, Grubeck-Loebenstein B, Heinz FX. Age affects quantity but not quality of antibody responses after vaccination with an inactivated flavivirus vaccine against tick-borne encephalitis. PLoS One 2012; 7: e34145.

https://doi.org/10.1371/journal.pone.0034145 DOI: https://doi.org/10.1371/journal.pone.0034145

Müller L, Andrée M, Moskorz W, Drexler I, Walotka L, Grothmann R, et al. Age-dependent immune response to the Biontech/Pfizer BNT162b2 coronavirus disease 2019 vaccination. Clin Infect Dis 2021; 73: 2065-2072.

https://doi.org/10.1093/cid/ciab381 DOI: https://doi.org/10.1093/cid/ciab381

Ahmed SF, Quadeer AA, McKay MR. SARS-CoV-2 T cell responses elicited by COVID-19 vaccines or infection are expected to remain robust against Omicron. Viruses 2022; 14: 79.

https://doi.org/10.3390/v14010079 DOI: https://doi.org/10.3390/v14010079

Seree-Aphinan C, Ratanapokasatit Y, Suchonwanit P, Rattanakaemakorn P, O-Charoen P, Pisitkun P, et al. Optimal time for COVID-19 vaccination in rituximab-treated dermatologic patients. Front Immunol 2023; 14: 1138765.

https://doi.org/10.3389/fimmu.2023.1138765 DOI: https://doi.org/10.3389/fimmu.2023.1138765

Seree-Aphinan C, Suchonwanit P, Rattanakaemakorn P, Pomsoong C, Ratanapokasatit Y, Setthaudom C, et al. Risk-benefit profiles associated with receiving Moderna COVID-19 (mRNA-1273) vaccine as an additional pre-booster dose in immune-mediated dermatologic disease patients with low SARS-CoV-2-specific immunity following the primary series: a prospective cohort study. J Eur Acad Dermatol Venereol 2023; 37: e572-e575.

https://doi.org/10.1111/jdv.18890 DOI: https://doi.org/10.1111/jdv.18890

Avallone G, Cavallo F, Astrua C, Caldarola G, Conforti C, De Simone C, et al. Cutaneous adverse reactions following SARS-CoV-2 vaccine booster dose: a real-life multicentre experience. J Eur Acad Dermatol Venereol 2022; 36: e876-e879.

https://doi.org/10.1111/jdv.18386 DOI: https://doi.org/10.1111/jdv.18386

Nakashima C, Kato M, Otsuka A. Cutaneous manifestations of COVID-19 and COVID-19 vaccination. J Dermatol 2023; 50: 280-289.

https://doi.org/10.1111/1346-8138.16651 DOI: https://doi.org/10.1111/1346-8138.16651

Maronese CA, Zelin E, Avallone G, Moltrasio C, Romagnuolo M, Ribero S, et al. Cutaneous vasculitis and vasculopathy in the era of COVID-19 pandemic. Front Med 2022; 9: 996288.

https://doi.org/10.3389/fmed.2022.996288 DOI: https://doi.org/10.3389/fmed.2022.996288

von Sonnenburg F, Perona P, Darsow U, Ring J, von Krempelhuber A, Vollmar J, et al. Safety and immunogenicity of modified vaccinia Ankara as a smallpox vaccine in people with atopic dermatitis. Vaccine 2014; 32: 5696-5702.

https://doi.org/10.1016/j.vaccine.2014.08.022 DOI: https://doi.org/10.1016/j.vaccine.2014.08.022

Boekel L, Stalman EW, Wieske L, Hooijberg F, van Dam KPJ, Besten YR, et al. Breakthrough SARS-CoV-2 infections with the delta (B.1.617.2) variant in vaccinated patients with immune-mediated inflammatory diseases using immunosuppressants: a substudy of two prospective cohort studies. Lancet Rheumatol 2022; 4: e417-e429.

Stalman EW, Wieske L, van Dam KPJ, Kummer LY, van Kempen ZLE, Killestein J, et al. Breakthrough infections with the SARS-CoV-2 omicron (B.1.1.529) variant in patients with immune-mediated inflammatory diseases. Ann Rheum Dis 2022; 81: 1757-1766.

https://doi.org/10.1136/ard-2022-222904 DOI: https://doi.org/10.1136/ard-2022-222904

Cao C, Qiu F, Lou C, Fang L, Liu F, Zhong J, et al. Safety of inactivated SARS-CoV-2 vaccines in patients with allergic diseases. Respir Res 2022; 23: 133.

https://doi.org/10.1186/s12931-022-02054-1 DOI: https://doi.org/10.1186/s12931-022-02054-1

Piros ÉA, Cseprekál O, Görög A, Hidvégi B, Medvecz M, Szabó Z, et al. Seroconversion after anti-SARS-CoV-2 mRNA vaccinations among moderate-to-severe psoriatic patients receiving systemic biologicals: prospective observational cohort study. Dermatol Ther 2022; 35: e15408.

https://doi.org/10.1111/dth.15408 DOI: https://doi.org/10.1111/dth.15408

Baloghová J, Kampe T, Kolarčik P, Hatalová E. Vaccination, risk factors and outcomes of COVID-19 infection in patients with psoriasis: a single centre real-life experience from eastern Slovakia. Viruses 2022; 14: 1646.

https://doi.org/10.3390/v14081646 DOI: https://doi.org/10.3390/v14081646

Published

2024-05-02

How to Cite

Chirasuthat, S., Ratanapokasatit, Y. ., Thadanipon, K. ., & Chanprapaph, K. . (2024). Immunogenicity, Effectiveness, and Safety of COVID-19 Vaccines among Patients with Immune-Mediated Dermatological Diseases: A Systematic Review and Meta-analysis. Acta Dermato-Venereologica, 104, adv40009. https://doi.org/10.2340/actadv.v104.40009