ReviewFrontiers in cellular neuroscience2026
Microglial PD-1/PD-L1 axis in CNS demyelinating diseases: a dual immunoregulatory perspective.
Review in Frontiers in cellular neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Multiple sclerosis (MS) and neuromyelitis optica spectrum disorder (NMOSD) stand as archetypal autoimmune-mediated demyelinating diseases of the central nervous system (CNS). Emerging evidence highlights the dual immunomodulatory functions of microglia in these diseases: on the one hand, they can secrete neurotoxic molecules that exacerbate neural damage; on the other hand, they are capable of releasing neuroprotective factors that promote tissue repair and enhance neuronal survival. This review dissects the programmed cell death ligand 1 (PD-L1)/programmed cell death protein 1 (PD-1) immune checkpoint axis, expressed on activated microglia, T cells, and other immune cells, as a pivotal rheostat of neuroinflammation. The binding of PD-1 to PD-L1 dampens immune cell activation and proliferation, curtails pro-inflammatory cytokine output, and is instrumental in preserving immune tolerance. In the context of chronic inflammation, persistent PD-1/PD-L1 signaling has been closely associated with the induction of T cell exhaustion than with direct apoptosis, though context-dependent effects on cell survival have been reported in certain experimental paradigms. Both microglia and the PD-1/PD-L1 axis are critically intertwined in the initiation and perpetuation of CNS demyelinating diseases. A more granular comprehension of their interplay will not only illuminate the molecular underpinnings of neuroinflammation and immune regulation in MS and NMOSD but also pave the way for crafting precision immunotherapies aimed at modulating microglial polarization. Here, we systematically review the dual immunomodulatory functions of the microglial PD-1/PD-L1 axis in these diseases and deliberate on the therapeutic prospects of targeting this pathway, thereby furnishing a conceptual framework for novel immune intervention strategies.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.