Evidence map›Paper›PMID 42200380›Full record

ArticleJournal of the European Academy of Dermatology and Venereology : JEADV2026

Tocilizumab for severe and refractory mucous membrane pemphigoid.

Billal Tedbirt, Maud Maho-Vaillant, Julie Gueudry, Marie-Laure Golinski, Marion Marcaillou, Blanche Bergeret, Guillaume Chambon, Pierre Bouchetemble, Soumeya Bekri, Abdellah Tebani and 11 more

Abstract read
In one paragraph

Article in Journal of the European Academy of Dermatology and Venereology : JEADV, 2026. 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
–field-weighted citation impact
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.

  1. Tocilizumab for severe and refractory mucous membrane pemphigoid.Journal of the European Academy of Dermatology and Venereology : JEADV · 2026
    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

21 authors.

Billal TedbirtDepartment of Dermatology, French Reference Center for Auto Immune Blistering Diseases, Rouen University Hospital, Normandie University, Rouen, France.
Maud Maho-VaillantUniv Rouen Normandie, Inserm, Normandie Univ, PANTHER UMR 1234, Rouen, France.
Julie GueudryDepartment of Ophthalmology, Rouen University Hospital, Rouen, France.ORCID https://orcid.org/0000-0002-8592-3810
Marie-Laure GolinskiUniv Rouen Normandie, Inserm, Normandie Univ, PANTHER UMR 1234, Rouen, France.
Marion MarcaillouDepartment of Dermatology, Toulouse University Hospital, Toulouse, France.
Blanche BergeretDepartment of Dermatology, CHU Nîmes, Nîmes, France.
Guillaume ChambonDepartment of Otolaryngology-Head and Neck Surgery, CHU Nîmes, Nîmes, France.
Pierre BouchetembleDepartment of Otolaryngology-Head and Neck Surgery, CHU Rouen, Rouen, France.
Soumeya BekriDepartment of Metabolic Biochemistry, Normandie University, UNIROUEN, INSERM U1245, CHU Rouen, Rouen, France.
Abdellah TebaniDepartment of Metabolic Biochemistry, Normandie University, UNIROUEN, INSERM U1245, CHU Rouen, Rouen, France.
Hervé MaillardDepartment of Dermatology, Hôpital du Mans, Le Mans, France.
Cécile MoriceDepartment of Dermatology, CHU Caen, Caen, France.
Anais VautierDepartment of Ophthalmology, Angers University Hospital, Angers, France.
Edgar-Pierre LibertDepartment of Dermatology, Angers University Hospital, Angers, France.
Christelle Le Roux-VilletDepartment of Dermatology & Reference Center for Autoimmune Bullous Diseases, Avicenne University Hospital, AP-HP, Sorbonne-Paris-Nord University, Bobigny, France.
Marion CarretteUniv Rouen Normandie, Inserm, Normandie Univ, PANTHER UMR 1234, Rouen, France.
Olivier BoyerUniv Rouen Normandie, Inserm, Normandie Univ, PANTHER UMR 1234, Rouen, France.
Vivien HébertDepartment of Dermatology, French Reference Center for Auto Immune Blistering Diseases, Rouen University Hospital, Normandie University, Rouen, France.ORCID https://orcid.org/0000-0001-9071-2033
Sébastien CalboUniv Rouen Normandie, Inserm, Normandie Univ, PANTHER UMR 1234, Rouen, France.
André GillibertDepartment of Biostatistics, CHU Rouen, Rouen, France.
Pascal JolyDepartment of Dermatology, French Reference Center for Auto Immune Blistering Diseases, Rouen University Hospital, Normandie University, Rouen, France.ORCID https://orcid.org/0000-0002-5734-0255

Funding

FIMARAD (Filière de Santé Maladies Rares Dermatologiques)Société Française de Dermatologie et de Pathologie Sexuellement Transmissible
6 · The paper itself

Abstract

backgroundMucous membrane pemphigoid (MMP) is a rare autoimmune blistering disease involving mucous membranes with a potentially devastating fibrosing course. Laryngotracheal and/or oesophageal involvement may lead to life-threatening complications, while corneal involvement may lead to blindness.

objectivesTo characterize the serum cytokine profile of MMP and to evaluate the efficacy of tocilizumab in nine cases of severe MMP according to the serum levels of IL-6.

methodsSera from MMP patients were compared to sex- and age-matched healthy donors (HD) and patients with bullous pemphigoid (BP), using two proteomic assays (Olink and Luminex). The Olink assay included 40 MMP, 40 BP and 40 HD sera, and the Luminex assay included 63 MMP, 31 BP and 24 HD sera. Based on these findings, nine patients with severe and refractory MMP received tocilizumab on a compassionate use basis after failure of standard therapies.

resultsProteomic analyses revealed high serum levels of IL-6, IL-8, MIP-1α/CCL3 and MIP-1β/CCL4 in MMP compared to BP and HD. Patients with MMP who achieved complete remission during follow-up had lower baseline serum levels of IL-6 (p < 0.0001), IL-8 (p = 0.0382), MIP-1α/CCL3 (p = 0.0005) and MIP-1β/CCL4 (p = 0.0009) than those with persistent disease activity. Nine patients with severe and refractory MMP were treated with tocilizumab. Their mean MMPDAI score decreased from 14.8 ± 6.6 to 4.2 ± 3.2 (p = 0.009). At the last evaluation, seven patients (78%) were in partial remission, one (11%) in complete remission and one (11%) recently treated achieved control of disease activity. Baseline IL-6 was elevated in five of eight tested patients; all three with normal IL-6 levels improved clinically. Four non-severe adverse events were observed (two neutropenias, one thrombocytopenia, one hepatic cytolysis).

conclusionsProteomic analyses identified a distinct MMP cytokine profile with increased IL-6, IL-8, MIP-1α/CCL3 and MIP-1β/CCL4, supporting IL-6 targeting, with tocilizumab as a potential option in severe refractory MMP.

Indexed as

Antibodies, Monoclonal, HumanizedPemphigoid, Benign Mucous MembraneAgedAged, 80 and overCytokinesFemaleHumansInterleukin-6MaleMiddle AgedProteomicsSeverity of Illness IndexAntibodies, Monoclonal, HumanizedCytokinesInterleukin-6tocilizumabbenign mucous membranebullous pemphigoidmucous membrane pemphigoidpemphigoidproteomicstocilizumab

Identifiers

PMID42200380
PMCPMC13613347

What Socratic 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 Socratic graph.