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Higher proinflammatory responses possibly contributing to suppressed cytotoxicity in patients with COVID-19 associated mucormycosis.
Shete, Ashwini; Deshpande, Supriya; Sawant, Jyoti; Warthe, Nidhi; Thakar, Madhuri; Madkaikar, Manisha; Pradhan, Vandana; Rao, Prajwal; Rohatgi, Shalesh; Mukherjee, Aparna; Anand, Tanu; Satija, Aanchal; Sharma Velamuri, Poonam; Das, Madhuchhanda; Deasi, Nidhi; Kumar Tembhurne, Alok; Yadav, Reetika; Pawaskar, Swapnal; Rajguru, Chhaya; Sankhe, Lalitkumar R; Chavan, Shrinivas S; Panda, Samiran.
  • Shete A; ICMR-National AIDS Research Institute (ICMR-NARI), Pune, India. Electronic address: ashete@nariindia.org.
  • Deshpande S; ICMR-National AIDS Research Institute (ICMR-NARI), Pune, India.
  • Sawant J; ICMR-National AIDS Research Institute (ICMR-NARI), Pune, India.
  • Warthe N; ICMR-National AIDS Research Institute (ICMR-NARI), Pune, India.
  • Thakar M; ICMR-National AIDS Research Institute (ICMR-NARI), Pune, India.
  • Madkaikar M; ICMR - National Institute of Immunohematology (ICMR-NIIH), Mumbai, India.
  • Pradhan V; ICMR - National Institute of Immunohematology (ICMR-NIIH), Mumbai, India.
  • Rao P; Dr. D. Y. Patil Medical College, Hospital & Research Centre, Dr. D. Y. Patil Vidyapeeth, Pune, India.
  • Rohatgi S; Dr. D. Y. Patil Medical College, Hospital & Research Centre, Dr. D. Y. Patil Vidyapeeth, Pune, India.
  • Mukherjee A; Indian Council of Medical Research, New Delhi, India.
  • Anand T; Indian Council of Medical Research, New Delhi, India.
  • Satija A; Indian Council of Medical Research, New Delhi, India.
  • Sharma Velamuri P; Indian Council of Medical Research, New Delhi, India.
  • Das M; Indian Council of Medical Research, New Delhi, India.
  • Deasi N; ICMR - National Institute of Immunohematology (ICMR-NIIH), Mumbai, India.
  • Kumar Tembhurne A; ICMR - National Institute of Immunohematology (ICMR-NIIH), Mumbai, India.
  • Yadav R; ICMR - National Institute of Immunohematology (ICMR-NIIH), Mumbai, India.
  • Pawaskar S; ICMR - National Institute of Immunohematology (ICMR-NIIH), Mumbai, India.
  • Rajguru C; Grant Government Medical College and J J group of Hospitals, Mumbai, India.
  • Sankhe LR; Grant Government Medical College and J J group of Hospitals, Mumbai, India.
  • Chavan SS; Grant Government Medical College and J J group of Hospitals, Mumbai, India.
  • Panda S; ICMR-National AIDS Research Institute (ICMR-NARI), Pune, India; Indian Council of Medical Research, New Delhi, India. Electronic address: samiranpanda.hq@icmr.gov.in.
Immunobiology ; 228(3): 152384, 2023 05.
Article in English | MEDLINE | ID: covidwho-2303646
ABSTRACT

INTRODUCTION:

COVID-19 Associated Mucormycosis (CAM), an opportunistic fungal infection, surged during the second wave of SARS Cov-2 pandemic. Since immune responses play an important role in controlling this infection in immunocompetent hosts, it is required to understand immune perturbations associated with this condition for devising immunotherapeutic strategies for its control. We conducted a study to determine different immune parameters altered in CAM cases as compared to COVID-19 patients without CAM.

METHODOLOGY:

Cytokine levels in serum samples of CAM cases (n = 29) and COVID-19 patients without CAM (n = 20) were determined using luminex assay. Flow cytometric assays were carried out in 20 CAM cases and 10 controls for determination of frequency of NK cells, DCs, phagocytes, T cells and their functionalities. The cytokine levels were analyzed for their association with each other as well as with T cell functionality. The immune parameters were also analyzed with respect to the known risk factors such as diabetes mellitus and steroid treatment.

RESULTS:

Significant reduction in frequencies of total and CD56 + CD16 + NK cells (cytotoxic subset) was noted in CAM cases. Degranulation responses indicative of cytotoxicity of T cell were significantly hampered in CAM cases as compared to the controls. Conversely, phagocytic functions showed no difference in CAM cases versus their controls except for migratory potential which was found to be enhanced in CAM cases. Levels of proinflammatory cytokines such as IFN-γ, IL-2, TNF-α, IL-17, IL-1ß, IL-18 and MCP-1 were significantly elevated in cases as compared to the control with IFN-γ and IL-18 levels correlating negatively with CD4 T cell cytotoxicity. Steroid administration was associated with higher frequency of CD56 + CD16- NK cells (cytokine producing subset) and higher MCP-1 levels. Whereas diabetic participants had higher phagocytic and chemotactic potential and had higher levels of IL-6, IL-17 and MCP-1.

CONCLUSION:

CAM cases differed from the controls in terms of higher titers of proinflammatory cytokines, reduced frequency of total and cytotoxic CD56 + CD16 + NK cell. They also had reduced T cell cytotoxicity correlating inversely with IFN-γ and IL-18 levels, possibly indicating induction of negative feedback mechanisms while diabetes mellitus or steroid administration did not affect the responses negatively.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Mucormycosis Type of study: Observational study / Prognostic study Topics: Variants Limits: Humans Language: English Journal: Immunobiology Year: 2023 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: COVID-19 / Mucormycosis Type of study: Observational study / Prognostic study Topics: Variants Limits: Humans Language: English Journal: Immunobiology Year: 2023 Document Type: Article