Evidence map›Paper›PMID 35445287›Full record

ArticleJournal of clinical immunology2022

The Impact of SARS-CoV-2 Infection in Patients with Inborn Errors of Immunity: the Experience of the Italian Primary Immunodeficiencies Network (IPINet).

Giuliana Giardino, Cinzia Milito, Vassilios Lougaris, Alessandra Punziano, Maria Carrabba, Francesco Cinetto, Riccardo Scarpa, Rosa Maria Dellepiane, Silvia Ricci, Beatrice Rivalta and 21 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of clinical immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.1field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 36 citations in OpenAlex.

  1. Trial
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  10. Severity of SARS-CoV-2 infection in children with inborn errors of immunity (primary immunodeficiencies): a systematic review.Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology · 2023
    Article
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  16. Selective IgA Deficiency May Be an Underrecognized Risk Factor for Severe COVID-19.The journal of allergy and clinical immunology. In practice · 2023
    Article
  17. Observational
  18. Article
  19. Article
  20. Detection of specific RBDFrontiers in immunology · 2023
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

31 authors at 13 institutions in 1 country.

Giuliana GiardinoDepartment of Translational Medical Sciences, Section of Pediatrics, Federico II University of Naples, Naples, Italy.
Cinzia MilitoDepartment of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Vassilios LougarisDepartment of Clinical and Experimental Sciences, Pediatrics Clinic and Institute for Molecular Medicine A. Nocivelli, University of Brescia, Brescia, Italy.
Alessandra PunzianoDepartment of Translational Medical Sciences, Center for Basic and Clinical Immunology Research, University of Naples Federico II, Naples, Italy.
Maria CarrabbaInternal Medicine Department, Rare Disease Unit, Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico, Milan, Italy.
Francesco CinettoRare Disease Referral Center, Internal Medicine 1, Ca Foncello Hospital, ULSS2 Marca Trevigiana, Treviso, Italy.
Riccardo ScarpaRare Disease Referral Center, Internal Medicine 1, Ca Foncello Hospital, ULSS2 Marca Trevigiana, Treviso, Italy.
Rosa Maria DellepianeDepartment of Pediatrics, Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico, Milan, Italy.
Silvia RicciDepartment of Health Sciences, University of Florence, Florence, Italy.
Beatrice RivaltaUnit of Immunology and Infectious Diseases, Academic Department of Pediatrics, Bambino Gesù Children's Hospital, Rome, Italy.
Francesca ContiUnit of Pediatrics, University of Bologna, St. Orsola University Hospital, Bologna, Italy.
Antonio MarzolloDepartment of Women's and Children's Health, Pediatric Hematology-Oncology Unit, University of Padua, Padua, Italy.
Davide FirinuDepartment of Medical Sciences and Public Health, University of Cagliari, Monserrato, Italy.
Emilia CirilloDepartment of Translational Medical Sciences, Section of Pediatrics, Federico II University of Naples, Naples, Italy.
Gianluca LagneseDepartment of Translational Medical Sciences, Center for Basic and Clinical Immunology Research, University of Naples Federico II, Naples, Italy.
Caterina CancriniUnit of Immunology and Infectious Diseases, Academic Department of Pediatrics, Bambino Gesù Children's Hospital, Rome, Italy.
Baldassare MartireUnit of Pediatrics and Neonatology, "Monsignor A.R. Dimiccoli" Hospital, Barletta, Italy.
Maria Giovanna DanieliClinica Medica, Dipartimento Di Scienze Cliniche E Molecolari, Università Politecnica Delle Marche E Azienda Ospedali Riuniti, Ancona, Italy.
Andrea PessionUnit of Pediatrics, University of Bologna, St. Orsola University Hospital, Bologna, Italy.
Angelo VaccaDepartment of Biomedical Sciences and Human Oncology, Section of Internal Medicine and Clinical Oncology, University of Bari Medical School, Bari, Italy.
Chiara AzzariDepartment of Health Sciences, University of Florence, Florence, Italy.
Giovanna FabioInternal Medicine Department, Rare Disease Unit, Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico, Milan, Italy.
Annarosa SoresinaDepartment of Clinical and Experimental Sciences, Pediatrics Clinic and Institute for Molecular Medicine A. Nocivelli, University of Brescia, Brescia, Italy.
Carlo AgostiniInternal Medicine Department, Rare Disease Unit, Fondazione IRCCS Ca Granda Ospedale Maggiore Policlinico, Milan, Italy.
Giuseppe SpadaroDepartment of Translational Medical Sciences, Center for Basic and Clinical Immunology Research, University of Naples Federico II, Naples, Italy.
Raffaele BadolatoDepartment of Clinical and Experimental Sciences, Pediatrics Clinic and Institute for Molecular Medicine A. Nocivelli, University of Brescia, Brescia, Italy.
Maria Pia CicalesePediatric Immunohematology and Bone Marrow Transplantation Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Alessandro AiutiPediatric Immunohematology and Bone Marrow Transplantation Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.
Alessandro PlebaniDepartment of Clinical and Experimental Sciences, Pediatrics Clinic and Institute for Molecular Medicine A. Nocivelli, University of Brescia, Brescia, Italy.
Isabella QuintiDepartment of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Claudio PignataDepartment of Translational Medical Sciences, Section of Pediatrics, Federico II University of Naples, Naples, Italy. pignata@unina.it.ORCID http://orcid.org/0000-0003-1568-9843
Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITUniversity of Naples Federico II · ITUniversity of Padua · ITMeyer Children's Hospital · ITSapienza University of Rome · ITUniversity of Bologna · ITUniversity of Rome Tor Vergata · ITVita-Salute San Raffaele University · ITFederico II University Hospital · ITMarche Polytechnic University · ITUniversity of Bari Aldo Moro · ITUniversity of Cagliari · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

COVID-19 manifestations range from asymptomatic to life-threatening infections. The outcome in different inborn errors of immunity (IEI) is still a matter of debate. In this retrospective study, we describe the experience of the of the Italian Primary Immunodeficiencies Network (IPINet). Sixteen reference centers for adult or pediatric IEI were involved. One hundred fourteen patients were enrolled including 35 pediatric and 79 adult patients. Median age was 32 years, and male-to-female ratio was 1.5:1. The most common IEI were 22q11.2 deletion syndrome in children (26%) and common variable immunodeficiency (CVID) in adults (65%). Ninety-one patients did not require hospital admission, and among these, 33 were asymptomatic. Hospitalization rate was 20.17%. Older age (p 0.004) and chronic lung disease (p 0.0008) represented risk factors for hospitalization. Hospitalized patients mainly included adults suffering from humoral immunodeficiencies requiring immunoglobulin replacement therapy and as expected had lower B cell counts compared to non-hospitalized patients. Infection fatality rate in the whole cohort was 3.5%. Seroconversion was observed is 86.6% of the patients evaluated and in 83.3% of CVID patients. 16.85% of the patients reported long-lasting COVID symptoms. All but one patient with prolonged symptoms were under IgRT. The fatality rate observed in IEI was slightly similar to the general population. The age of the patients who did not survive was lower compared to the general population, and the age stratified mortality in the 50-60 age range considerable exceeded the mortality from 50 to 60 age group of the Italian population (14.3 vs 0.6%; p < 0.0001). We hypothesize that this is due to the fact that comorbidities in IEI patients are very common and usually appear early in life.

Indexed as

Common Variable ImmunodeficiencyCOVID-19AdultChildFemaleHospitalizationHumansMalePost-Acute COVID-19 SyndromeRetrospective StudiesSARS-CoV-2COVID-19Inborn errors of immunityOutcomeSARS-CoV-2SeroconversionViral shedding

Identifiers

PMID35445287
PMCPMC9020753
OpenAlexW4224212011

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