Evidence map›Paper›PMID 37001437›Full record

Observational studyJournal of autoimmunity2023

Outcome of SARS-CoV2 infection in hematopoietic stem cell transplant recipients for autoimmune diseases.

Raffaella Greco, John A Snowden, Nina Simone Knelange, Gloria Tridello, Carlotta Cacciatore, Alienor Xhaard, Fabio Ciceri, Matthew Collin, Christelle Ferra, Ann De Becker and 6 more

Open access · hybridAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in Journal of autoimmunity, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Review
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

16 authors at 14 institutions in 9 countries.

Raffaella GrecoUnit of Hematology and Bone Marrow Transplantation, IRCCS San Raffaele Hospital, Vita-Salute San Raffaele University, Milan, Italy. Electronic address: greco.raffaella@hsr.it.
John A SnowdenDepartment of Haematology, Sheffield Teaching Hospitals Foundation NHS Trust, Sheffield, United Kingdom.
Nina Simone KnelangeEBMT - Leiden Study Unit, Leiden, Netherlands.
Gloria TridelloPaediatric Haematology Oncology, Azienda Ospedaliera Universitaria Integrata, Verona, Italy.
Carlotta CacciatoreUnité de Médecine Interne (UF04): CRMR MATHEC, Maladies Auto-immunes et Thérapie Cellulaire, Centre de Référence des Maladies Auto-immunes Systémiques Rares d'Ile-de-France, AP-HP, Hôpital St-Louis, F-75010, Paris, France.
Alienor XhaardHôpital Saint-Louis, Department of Hematology - BMT, Paris, France.
Fabio CiceriUnit of Hematology and Bone Marrow Transplantation, IRCCS San Raffaele Hospital, Vita-Salute San Raffaele University, Milan, Italy.
Matthew CollinNorthern Centre for Bone Marrow Transplantation, Newcastle Upon Tyne Hospitals NHS Foundation Trust, Newcastle, UK.
Christelle FerraICO-Hospital Universitari Germans Trias i Pujol, Badalona, Spain.
Ann De BeckerUniversitair Ziekenhuis Brussel, Brussels, Belgium.
Manuela BadoglioEBMT Paris Study Office / CEREST-TC - Department of Haematology, Saint Antoine Hospital - INSERM UMR 938 - Université Pierre et Marie Curie, Paris, France.
Dina AverbuchFaculty of Medicine, Hebrew University of Jerusalem, Hadassah Medical Center, Jerusalem, Israel.
Tobias AlexanderCharité - Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, And Berlin Institute of Health, Department of Rheumatology and Clinical Immunology, Berlin, Germany.
Per LjungmanDepartment of Cellular Therapy and Allogeneic Stem Cell Transplantation, Karolinska Comprehensive Cancer Center, Karolinska University Hospital Huddinge, Stockholm, Sweden; Division of Hematology, Department of Medicine Huddinge, Karolinska Institutet, Stockholm, Sweden.
Rafael De la CamaraDepartment of Hematology, Hospital de La Princesa, Madrid, Spain.
European Society for Blood and Marrow Transplantation (EBMT) COVID19 Task Force, Autoimmune Diseases Working Party (ADWP) and Infectious Diseases Working Party (IDWP)
Vita-Salute San Raffaele University · ITAssistance Publique – Hôpitaux de Paris · FRAzienda Ospedaliera Universitaria Integrata Verona · ITEuropean Society for Blood and Marrow Transplantation · NLHebrew University of Jerusalem · ILHôpital Saint-Louis · FRHospital Universitari Germans Trias i Pujol · ESHospital Universitario de La Princesa · ESHumboldt-Universität zu Berlin · DEInserm · FRKarolinska University Hospital · SENewcastle upon Tyne Hospitals NHS Foundation Trust · GBSheffield Teaching Hospitals NHS Foundation Trust · GBUniversitair Ziekenhuis Brussel · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Hematopoietic stem cell transplant (HSCT) recipients may be at high risk of mortality from coronavirus disease 2019 (COVID-19). However, specific data on COVID-19 after treatment with HSCT in patients affected by autoimmune diseases (ADs) are still lacking. In this multicenter observational study of the European Society for Blood and Marrow Transplantation (EBMT), clinical data on COVID-19 in 11 patients affected by severe ADs treated with HSCT (n = 3 allogeneic transplant; n = 8 autologous transplant) are reported. All patients were symptomatic during the initial phase of the SARS-CoV-2 infection. At screening, 5 patients reported upper respiratory symptoms, 3 patients had cough without oxygen requirement, and 6 patients exhibited extra-pulmonary symptoms. Four cases developed a lower respiratory tract disease (LRTD). Hospitalization was required in 6 cases, without necessity of intensive care unit (ICU) admission and/or ventilation/supplemental oxygen. Different interventions were adopted: remdesivir (n = 1), nirmatrelvir/ritonavir (n = 1), sotrovimab (n = 1), immunoglobulins (n = 1). At last follow-up, all patients are alive and had resolution of the infection. The current analysis describing the mild-moderate course of COVID-19 in transplant recipients affected by ADs, similar to the course observed in ADs under standard treatments, provides useful information to support the delivery of HSCT programs in this field. Vaccination and new treatments available for SARS-CoV-2 may be useful to further minimize the risk of infection.

Indexed as

Autoimmune DiseasesCOVID-19Hematopoietic Stem Cell TransplantationHumansRNA, ViralSARS-CoV-2Transplant RecipientsRNA, ViralAutoimmune diseasesCOVID-19Hematopoietic stem cell transplantSARS-CoV-2Survival

Identifiers

PMID37001437
PMCPMC9977622
OpenAlexW4322773659

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.