Evidence map›Paper›PMID 26417354›Full record

ArticleEXCLI journal2015

Rituximab therapy improves recalcitrant Pemphigus vulgaris.

Pedram Noormohammadpour, Amirhooshang Ehsani, Hossein Mortazavi, Maryam Daneshpazhooh, Kamran Balighi, Mohammad Mofidi, Fatemeh Gholamali, Ali Sadeghinia

Open access · greenAbstract read
In one paragraph

Article in EXCLI journal, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

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

8 authors at 2 institutions in 1 country.

Pedram NoormohammadpourDepartment of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran ; Bullous Research Center, Tehran University of Medical Sciences, Tehran, Iran.
Amirhooshang EhsaniDepartment of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Hossein MortazaviDepartment of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Maryam DaneshpazhoohDepartment of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Kamran BalighiDepartment of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Mohammad MofidiDepartment of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Fatemeh GholamaliDepartment of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Ali SadeghiniaDepartment of Dermatology, Razi Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Razi Hospital · IRTehran University of Medical Sciences · IR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Pemphigus is a severe life-threatening blistering disease associated with autoantibodies against cell adhesion proteins desmogleins 1 and 3. Patients with severe pemphigus commonly show high rates of relapse after conventional immunosuppressive therapy. The newly developed drug Rituximab showed impressing promises in the treatment of refractory pemphigus vulgaris (PV). In the present study the efficacy of a single course rituximab therapy in the treatment of PV was investigated. Eighteen patients with severe recalcitrant PV were recruited to this study. Pemphigus disease activity index (PDAI), anti-desmoglein 1 and anti-desmoglein 3 antibody titers, and percent of CD20 positive cells were measured at baseline, 10 ± 1, and 22 ± 2 weeks after rituximab therapy. Rituximab was given intravenously at dose 375 mg/m(2) once weekly for 4 weeks. Rituximab therapy caused a dramatic reduction in the PDAI, accompanied by decreases in anti-desmoglein 1 and anti-desmoglein 3 antibody titers over the follow-up course. The B-cell population decreased at the first follow-up, but returned to its baseline levels at the second follow-up. Rituximab therapy decreased the dose of immunosuppressive drugs required to control the disease. It seems that the rituximab may be effective and safe for treatment of refractory PV.

Indexed as

anti-desmoglein 1 antibodyCD20 positive cellsnti-desmoglein 3 antibodyPemphigus vulgarisRituximab

Identifiers

PMID26417354
PMCPMC4553899
OpenAlexW566715556

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Registered trials

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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.