Evidence map›Paper›PMID 34668842›Full record

ArticleHuman vaccines & immunotherapeutics2021

Product review on MAbs (alemtuzumab and ocrelizumab) for the treatment of multiple sclerosis.

Tereza Gabelić, Barbara Barun, Ivan Adamec, Magdalena Krbot Skorić, Mario Habek

Abstract read
In one paragraph

Article in Human vaccines & immunotherapeutics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Remote loading of an autoantigen in PLGA nanoparticles for the treatment of multiple sclerosis.Journal of controlled release : official journal of the Controlled Release Society · 2025
    Article
  2. Observational
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. 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

5 authors.

Tereza GabelićDepartment of Neurology, University Hospital Center Zagreb, Zagreb, Croatia.
Barbara BarunDepartment of Neurology, University Hospital Center Zagreb, Zagreb, Croatia.
Ivan AdamecDepartment of Neurology, University Hospital Center Zagreb, Zagreb, Croatia.
Magdalena Krbot SkorićDepartment of Neurology, University Hospital Center Zagreb, Zagreb, Croatia.
Mario HabekDepartment of Neurology, University Hospital Center Zagreb, Zagreb, Croatia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Traditionally, the management of active relapsing remitting MS was based on the, so-called, maintenance therapy, which is characterized by continuous treatment with particular disease modifying therapy (DMT), and a return of disease activity when the drug is discontinued. Another approach is characterized by a short treatment course of a DMT, which is hypothesized to act as an immune reconstitution therapy (IRT), with the potential to protect against relapses for years after a short course of treatment. Introduction of monoclonal antibodies in the treatment of MS has revolutionized MS treatment in the last decade. However, given the increasingly complex landscape of DMTs approved for MS, people with MS and neurologists are constantly faced with the question which DMT is the most appropriate for the given patient, a question we still do not have an answer to. In this product review, we will discuss the first DMT that acts as IRT, an anti-CD52 monoclonal antibody alemtuzumab and an anti CD20 monoclonal antibody, ocrelizumab that has the potential to act as an IRT, but is administered continuously. Special emphasis will be given on safety in the context of COVID-19 pandemics and vaccination strategies.

Indexed as

COVID-19Multiple SclerosisMultiple Sclerosis, Relapsing-RemittingAlemtuzumabAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedHumansImmunologic FactorsSARS-CoV-2AlemtuzumabAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedImmunologic Factorsocrelizumabalemtuzumabdisease modifying therapymonoclonal antibodiesMultiple sclerosisocrelizumab

Identifiers

PMID34668842
PMCPMC8828070

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.