Rohit Saluja

Dr. Rohit Saluja

orcid

Research Focus & Metrics

Academic Career Length

11Years (2016-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
13 August 2018 in Frontiers in Immunology
Verified
Journal Article
Open access
PDF file
ETElden Berla Thangam
Elden Berla Thangam
EJEbenezer Angel Jemima
Ebenezer Angel Jemima
HSHimadri Singh
Himadri Singh
MBMirza Saqib Baig
Mirza Saqib Baig
MKMahejibin Khan
Mahejibin Khan
RSRohit Saluja
Rohit Saluja
Histamine and its receptors (H1R–H4R) play a crucial and significant role in the development of various allergic diseases. Mast cells are multifunctional bone marrow-derived tissue-dwelling cells that are the major producer of histamine in the body. H1R are expressed in many cells, including mast cells, and are involved in Type 1 hypersensitivity reactions. H2R are involved in Th1 lymphocyte cytokine production. H3R are mainly involved in blood–brain barrier function. H4R are highly expressed on mast cells where their stimulation exacerbates histamine and cytokine generation. Both H1R and H4R have important roles in the progression and modulation of histamine-mediated allergic diseases. Antihistamines that target H1R alone are not entirely effective in the treatment of acute pruritus, atopic dermatitis, allergic asthma, and other allergic diseases. However, antagonists that target H4R have shown promising effects in preclinical and clinical studies in the treatment of several allergic diseases. In the present review, we examine the accumulating evidence suggesting novel therapeutic approaches that explore both H1R and H4R as therapeutic targets for histamine-mediated allergic diseases.

1 January 2018 in Oxidative Medicine and Cellular Longevity
Verified
Journal Article
Open access
PDF file
Mohamed Abdel-DaimMohamed Abdel-Daim
Mohamed Abdel-Daim
Khaled Abo-EL-SooudKhaled Abo-EL-Sooud
Khaled Abo-EL-Sooud
LALotfi Aleya
Lotfi Aleya
Simona BungăuSimona Bungău
Simona Bungău
Agnieszka Barbara NajdaAgnieszka Barbara Najda
Agnieszka Barbara Najda
RSRohit Saluja
Rohit Saluja

1 May 2016 in European Journal of Pharmacology
Verified
Journal Article
Closed access
RSRohit Saluja
Rohit Saluja
AZAnna Zoltowska
Anna Zoltowska
MKMaria Elizabeth Ketelaar
Maria Elizabeth Ketelaar
GNGunnar Nilsson
Gunnar Nilsson

1 May 2023 in Indian Journal of Medical Research
Verified
Journal Article
Open access
HSHimadri Singh
Himadri Singh
SKSagar Khadanga
Sagar Khadanga
SGSudhir K. Goel
Sudhir K. Goel
SMSyamantak Majumder
Syamantak Majumder
MBMirza S. Baig
Mirza S. Baig
RSRohit Saluja
Rohit Saluja
Background & objectives: Diabetes mellitus (DM) is characterized by increase in blood glucose levels due to defective insulin secretion or insulin sensitivity. Interleukins (ILs) are known to play an important role in the pathogenesis of DM. The aim of this study was to investigate the serum concentration of IL-33 and its receptor soluble ST2 (sST2) in patients with diabetes and draw a correlation between their serum levels and different standard glycaemic indices of patients affected with type-2 diabetes with or without metabolic syndrome. Methods: Thirty type-2 diabetic individuals and 30 healthy controls were recruited for this study. Serum and plasma were separated by centrifugation of blood for quantitative measurement of IL-33, sST2 and other biochemical parameters. Results: It was observed that serum IL-33 levels were significantly less and sST2 levels were significantly high in type-2 diabetic individuals as compared to healthy controls. A significant correlation between the serum IL-33 concentration and fasting plasma glucose (FPG) and postprandial plasma glucose (PPG) levels were also found. Additionally, data also elucidated that serum levels of high-density lipoprotein, low-density lipoprotein or triglyceride in type-2 diabetics did not influence the serum levels of IL-33 and sST2, thereby excluding these factors as the major drivers of changes in serum IL-33 and sST2 concentration. Interpretation & conclusions: This study demonstrated alteration in serum levels of IL-33 and sST2 in type-2 diabetic individuals. Further mechanistic studies, focusing on the progression of type-2 diabetes could elucidate the involvement of IL-33 in the cellular acquisition of insulin resistance as observed in type-2 diabetics.

1 April 2021 in Heliyon
Verified
Journal Article
Open access
NPNeeraj Pal
Neeraj Pal
AMAnil Kumar Mavi
Anil Kumar Mavi
SKSundip Kumar
Sundip Kumar
UKUmesh Kumar
Umesh Kumar
MJMaya Datt Joshi
Maya Datt Joshi
RSRohit Saluja
Rohit Saluja
The prevalence of COVID-19 continues to rise with more than 114,315,846 million confirmed cases and 2,539,427 deaths worldwide by 3 March 2021 and this number kept on increasing day by day. There is no clear therapeutic treatment or vaccine available for COVID-19 till date and by seeing such a high rise in the cases of COVID-19 on daily basis, it would have been necessary to implement precautions and hygienic measures to monitor and reduce human-to-human transmission of SARS-CoV-2 before there is any successful intervention/treatment available. Currently, several studies demonstrated the important improvements in both the innate and adaptive immune systems of COVID-19 patients. In particular, pre-existing research, on immune response to B cell and T cells are highlighting that pre-existing immunity exists in about 90% of the general population because of previous exposure to CoVs and having immunity against these CoVs. Although it is not clear from, the current studies on COVID-19 but it assumed that, it might have implication to COVID-19 severity and could play an important role in treatment or vaccine development against COVID-19. This review summarizes the information from occurrence of SARS-CoV-2 to its pathogenesis, transmission, adaptive immune response with respect to T cell and B cell stimulation and therapeutic interventions/treatment against COVID-19.