# VDLIN: A Deep Learning‐Based Platform for Methylcobalamin‐Inspired Immunomodulatory Compound Screening

**Authors:** Xuefei Guo, Yang Zhao, Xianle Rong, Chenxi Niu, Shiyu Hu, Qiang Liu, Fuping You

PMC · DOI: 10.1002/advs.202413775 · Advanced Science · 2025-10-27

## TL;DR

A new deep learning platform identifies a compound that balances anti-inflammatory and immune-boosting effects, potentially improving treatments for inflammatory diseases and SARS-CoV-2.

## Contribution

VDLIN is a novel deep learning model that screens compounds with dual anti-inflammatory and immune-stimulatory properties.

## Key findings

- VDLIN identified Co7, a compound that retains MCB's anti-inflammatory effects while enhancing immune activation.
- Co7 activates the TLR4 signaling pathway, offering a balanced immune modulation.
- The study reveals how chromatin dynamics influence immune regulation and therapeutic outcomes.

## Abstract

During the COVID‐19 pandemic, methylcobalamin (MCB), an active form of Vitamin B12 (VB12), showed therapeutic potential in mitigating the cytokine storm associated with SARS‐CoV‐2 infection. While MCB's significant anti‐inflammatory properties are confirmed, it is also observed that its treatment may impair macrophage‐mediated innate immune responses. Comprehensive RNA‐seq, ATAC‐seq, and CUT&Tag analyses revealed that MCB reduces inflammation and weakens innate immunity by limiting chromatin accessibility at NF‐κB and EGR1 binding sites, leading to decreased IFNB1 production and enhanced viral immune evasion. To address this challenge, a deep learning model, VDLIN (Vitamin B12‐derived Deep Learning for Innate Immunity), is developed to identify compounds capable of both suppressing inflammation and boosting innate immunity. As anticipated, VDLIN identified a novel compound, “Co7,” which retains MCB's strong anti‐inflammatory effects while also enhancing immune activation via the TLR4 signaling pathway. Co7 thus emerges as a promising therapeutic candidate, offering advantages over MCB by balancing anti‐inflammatory and immune‐stimulatory functions. Taken together, this study sheds light on the intricate interplay between chromatin dynamics and immune regulation, presenting new opportunities for therapeutic interventions in inflammatory diseases and SARS‐CoV‐2 infection.

Using the convolutional neural network model VDLIN, Co7 is identified as a promising therapeutic candidate. Co7 demonstrates distinct advantages over MCB by effectively balancing anti‐inflammatory and immune‐stimulatory functions, making it a potential novel approach for immune modulation.

## Linked entities

- **Genes:** NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790], EGR1 (early growth response 1) [NCBI Gene 1958], IFNB1 (interferon beta 1) [NCBI Gene 3456]
- **Chemicals:** methylcobalamin (PubChem CID 6436232), Co7 (PubChem CID 24894160)

## Full-text entities

- **Genes:** NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, EGR1 (early growth response 1) [NCBI Gene 1958] {aka AT225, G0S30, KROX-24, NGFI-A, TIS8, ZIF-268}, IFNB1 (interferon beta 1) [NCBI Gene 3456] {aka IFB, IFF, IFN-beta, IFNB}
- **Diseases:** COVID-19 (MESH:D000086382), VDLIN (MESH:D014806), inflammation (MESH:D007249)
- **Chemicals:** MCB (MESH:C019476), VB12 (MESH:D014805), Co7 (-)

## Full text

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## Figures

7 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12866821/full.md

## References

64 references — full list in the complete paper: https://tomesphere.com/paper/PMC12866821/full.md

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Source: https://tomesphere.com/paper/PMC12866821