Evidence map›Paper›PMID 38980318›Full record

ReviewExpert opinion on investigational drugs2024

Emerging treatment landscape for Guillain-Barré Syndrome (GBS): what's new?

Alina Sprenger-Svačina, Martin K R Svačina, Tong Gao, Gang Zhang, Kazim A Sheikh

Abstract readReview
In one paragraph

Review in Expert opinion on investigational drugs, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Acute Management of Guillain-Barré Syndrome: A Narrative Review.Archives of internal medicine research · 2026
    Article
  2. Article
  3. Article
  4. Review
  5. 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

5 authors.

Alina Sprenger-SvačinaDepartment of Neurology, University of Texas Health Science Center at Houston, Houston, TX, USA.
Martin K R SvačinaDepartment of Neurology, University of Texas Health Science Center at Houston, Houston, TX, USA.
Tong GaoDepartment of Neurology, University of Texas Health Science Center at Houston, Houston, TX, USA.
Gang ZhangDepartment of Neurology, University of Texas Health Science Center at Houston, Houston, TX, USA.
Kazim A SheikhDepartment of Neurology, University of Texas Health Science Center at Houston, Houston, TX, USA.

Funding

Modulation of CSF1R Signaling to Treat Inflammatory NeuropathiesR01NS134989 · NINDS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI KAZIM A SHEIKH · 2024 to 2026
$1.7M
NINDS NIH HHS R01 NS134989
6 · The paper itself

Abstract

introductionGuillain-Barré syndrome (GBS) is a monophasic immune neuropathic disorder characterized by acute paralysis. A significant portion of patients are left with residual deficits, which presents a considerable global healthcare challenge. The precise mechanisms underlying GBS pathogenesis are not fully elucidated. Recent studies have focused on postinfectious molecular mimicry and identified involvement of IgG autoantibodies and innate immune effectors in GBS. Intravenous immunoglobulins (IVIg) and plasma exchange (PE) are two established evidence-based immunomodulatory treatments for GBS, but a significant proportion of GBS patients fails to respond adequately to either therapy. This emphasizes an urgent need for novel and more potent treatments. AREAS COVERED: We discuss novel immunomodulatory therapies presently at different phases of preclinical and clinical investigation. Some drugs in development target pathophysiologic mechanisms such as IgG autoantibody catabolism and complement activation, which are relevant to GBS. EXPERT OPINION: There is an unmet need for more effective immune therapies for GBS. New immunomodulatory therapies under development may provide more potent options for GBS patients who do not respond to IVIg or PE. Future directions may include incorporating neuroprotective interventions based on evolving understanding of mechanisms underlying nerve injury and axonal degeneration.

Indexed as

Drug DevelopmentGuillain-Barre SyndromeImmunoglobulins, IntravenousPlasma ExchangeAnimalsAutoantibodiesHumansImmunity, InnateImmunoglobulin GImmunologic FactorsImmunomodulating AgentsMolecular MimicryNeuroprotective AgentsAutoantibodiesImmunoglobulin GImmunoglobulins, IntravenousImmunologic FactorsImmunomodulating AgentsNeuroprotective AgentscomplementFc-gamma receptorsGBSIgG autoantibodiesimmunomodulatory treatmentsIVIgNeonatal Fc receptor (FcRn)neuroprotective strategy

Identifiers

PMID38980318
PMCPMC11424254

What OpenQuestion holds

Textmetadata
LicenceTDM
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.