Chronic hyperglycemia drives alterations in macrophage effector function in pulmonary tuberculosis

ABSTRACT Background The rising prevalence of Diabetes mellitus (DM) in high TB endemic countries has the potential to adversely affect sustainability of TB control since DM can lead to alterations in both innate and adaptive immune response constituting as a risk factor for development of active tuberculosis (TB). The impact of hyperglycemia on TB specific innate immune response in terms of macrophage functions remains poorly addressed.Material and methods Macrophage effector functions in diabetic and non-diabetic individuals with and without PTB infection as well as non-diabetic-uninfected controls (fifty individuals in each group) were assessed. Phagocytic capacity against BCG and surface expression of PRRs (CD11b, CD14, CD206, MARCO and TLR2) were measured via flow cytometry. Effector molecules (ROS and NO) were assessed via DCFDA and Griess reaction respectively.Results A systematic dysregulation in phagocytic capacity with concurrent alterations in expression pattern of key PRRs (CD11b, MARCO and CD206) and effector molecules (ROS and NO) was observed in diabetic individuals with PTB. These altered macrophage functions were positively correlated with increase in disease severity in diabetic individuals.Conclusion Our results highlight several key patterns of immune dysregulation against M.Tb under hyperglycemic conditions. A significant reduction in macrophage effector functions in infected diabetic individuals which further correlated with increase in disease severity reveals a negative impact of hyperglycemia with aetiology and pathological progression of TB..

Medienart:

Preprint

Erscheinungsjahr:

2022

Erschienen:

2022

Enthalten in:

bioRxiv.org - (2022) vom: 28. Okt. Zur Gesamtaufnahme - year:2022

Sprache:

Englisch

Beteiligte Personen:

Panda, Sudhasini [VerfasserIn]
Seelan, Diravya M [VerfasserIn]
Faisal, Shah [VerfasserIn]
Luthra, Kalpana [VerfasserIn]
Palanichamy, Jayanth Kumar [VerfasserIn]
Mohan, Anant [VerfasserIn]
Vikram, Naval K [VerfasserIn]
Gupta, Neeraj Kumar [VerfasserIn]
Ramakrishnan, Lakshmy [VerfasserIn]
Singh, Archana [VerfasserIn]

Links:

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Themen:

570
Biology

doi:

10.1101/2022.01.18.476721

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

XBI035022841