Evidence map›Paper›PMID 41663643›Full record

ArticleIndian journal of gastroenterology : official journal of the Indian Society of Gastroenterology2026

AXL-dependent autophagy impairment differentiates monocyte-derived macrophages from Crohn's disease and intestinal tuberculosis.

Sonakshi Udinia, Mrinmoy Das, Shaina Jamwal, Manasvini Markandey, Aditya Bajaj, Lalita Mehra, Saurabh Kedia, Carey F H Lim, Shihui Foo, Prasenjit Das and 5 more

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Article in Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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.

No citing paper in PubMed yet.

4 · The record

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5 · Who and what money

Authors and funding

15 authors.

Sonakshi UdiniaCellular Immunology Group, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi, 110 067, India.
Mrinmoy DasCellular Immunology Group, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi, 110 067, India.
Shaina JamwalCellular Immunology Group, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi, 110 067, India.
Manasvini MarkandeyDepartment of Gastroenterology, All India Institute of Medical Sciences, New Delhi, 110 029, India.
Aditya BajajDepartment of Gastroenterology, All India Institute of Medical Sciences, New Delhi, 110 029, India.
Lalita MehraDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, 110 029, India.
Saurabh KediaDepartment of Gastroenterology, All India Institute of Medical Sciences, New Delhi, 110 029, India.
Carey F H LimA*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
Shihui FooSingapore Immunology Network (SIgN), A*STAR, Singapore, Singapore.
Prasenjit DasDepartment of Pathology, All India Institute of Medical Sciences, New Delhi, 110 029, India.
Shanshan HowlandSingapore Immunology Network (SIgN), A*STAR, Singapore, Singapore.
Mrutyunjay SuarSchool of Biotechnology, Kalinga Institute of Industrial Technology, Bhubaneswar, 751 024, India.
Amit SinghalA*STAR Infectious Diseases Labs (A*STAR ID Labs), Agency for Science, Technology and Research (A*STAR), Singapore, Singapore.
Vineet AhujaDepartment of Gastroenterology, All India Institute of Medical Sciences, New Delhi, 110 029, India. vineet.aiims@gmail.com.
Dhiraj KumarCellular Immunology Group, International Centre for Genetic Engineering and Biotechnology, Aruna Asaf Ali Marg, New Delhi, 110 067, India. dhiraj@icgeb.res.in.ORCID http://orcid.org/0000-0001-7578-2930

Funding

Flagship program from the Department of Biotechnology BT/IC-06/003/91Science and Engineering Research Board (SERB), Govt. of India EMR/2016/000026The Wellcome Trust DBT India Alliance IA/S/17/1/503071
6 · The paper itself

Abstract

backgroundMacrophages are critical to maintaining intestinal homeostasis and contribute to localized inflammation once dysregulated. Here, we aimed at understanding innate macrophage dysfunction in subjects with chronic idiopathic gut inflammation Crohn's disease (CD) and chronic infection-related gut inflammation, intestinal tuberculosis (ITB). METHODOLOGY: The study population involved subjects aged 18 years or above, including males and females, who met the inclusion/exclusion criteria (CD: n = 42; ITB: n = 41). RNA-seq analysis of ex vivo Mtb-infected or uninfected monocyte-derived macrophages (MDMs) from CD, ITB and healthy controls was done. The MDMs from a cohort of patients, including CD (n = 42) and ITB (n = 41), were characterized for innate immune responses such as autophagy (CD, n = 15: ITB, n = 09), mitochondrial depolarization (CD, n = 08: ITB, n = 08) and bactericidal capacity (CD, n = 25: ITB, n = 28). Finally, the role of AXL downregulation in impaired autophagy was tested.

resultsThe MDMs from CD and ITB subjects showed differential regulation of autophagy-associated genes. Functionally, CD MDMs showed significant autophagy impairment compared to ITB MDMs (average MFI-201 in CD vs. 414 in ITB). Both CD and ITB MDMs were permissive to Mtb uptake; however, CD MDMs were more permissive (44% CD samples vs. 28% ITB samples). We noted that AXL was consistently downregulated in CD MDMs and biopsies compared to ITB. AXL knockdown in macrophages impaired autophagy, suggesting a causal relationship between AXL expression and impaired autophagy in CD MDMs.

conclusionWe experimentally demonstrate distinct autophagy regulation between CD and ITB MDMs. Impaired autophagy in CD MDMs could explain the heightened chronic inflammation observed in CD subjects. The association of AXL downregulation with autophagy impairment could facilitate novel diagnostic and intervention approaches against CD.

Indexed as

AutophagyCrohn DiseaseMacrophagesProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesTuberculosis, GastrointestinalAdultAxl Receptor Tyrosine KinaseDown-RegulationFemaleHumansImmunity, InnateMaleMiddle AgedAxl Receptor Tyrosine KinaseProto-Oncogene ProteinsReceptor Protein-Tyrosine KinasesAutophagyCrohn’s diseaseInfectionInflammationTuberculosis

Identifiers

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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.