1. Immunophenotyping and Transcriptional Profiling of Human Plasmablasts in Dengue
- Author
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Pragati Sharma, Mohit Singla, Kamalvishnu P. Gottimukkala, Rakesh Lodha, Pushpendra Singh, Sivaram Gunisetty, Sanjeev Kumar, Priya Bhatnagar, Anmol Chandele, Guruprasad R. Medigeshi, Harekrushna Panda, Kaja Murali-Krishna, Yadya M Chawla, Kaustuv Nayak, Charu Aggarwal, Rafi Ahmed, Carl W. Davis, Sushil K. Kabra, Keshav Saini, Elluri Seetharami Reddy, Haydn T. Kissick, and Deepti Maheshwari
- Subjects
Chemokine ,Plasma Cells ,Immunology ,Population ,B-Lymphocyte Subsets ,India ,Cellular Response to Infection ,Antibodies, Viral ,Microbiology ,Immunophenotyping ,Dengue fever ,Dengue ,Chemokine receptor ,Virology ,medicine ,Humans ,Antibody-dependent enhancement ,education ,B cell ,B-Lymphocytes ,education.field_of_study ,biology ,business.industry ,Dengue Virus ,medicine.disease ,Antibody-Dependent Enhancement ,Phenotype ,Vaccination ,medicine.anatomical_structure ,Insect Science ,biology.protein ,Cytokines ,Antibody ,business - Abstract
Previous studies have shown that plasmablasts expand massively in dengue patients as compared to many other situations such as influenza infection or vaccination. However, a detailed understanding of the phenotypes and transcriptional features of these cells is lacking. Moreover, despite India having nearly a third of global dengue disease burden, there is virtually no information on plasmablasts responses in dengue patients from India. Here, we provide a detailed characterization of plasmablast responses from dengue confirmed febrile children in India. Immunophenotyping and RNA seq analysis showed that in addition to secreting dengue specific antibodies, these massively expanding cells expressed several adhesion molecules, chemokines and chemokine receptors that are involved in endothelial interactions, homing to skin or mucosal tissues including intestine. Surprisingly, we found that these cells also upregulated expression of several cytokine genes that are involved in angiogenesis, leukocyte extravasation and vascular permeability. These transcriptional features were qualitatively similar to plasmablasts from influenza vaccinees. Interestingly, the expansion of the plasmablasts in dengue patients was significantly lower in patients with primary dengue infection compared to those with secondary dengue. Moreover, within the primary dengue patients, their expansion was significantly lower in patients with mild dengue infection (DI) compared to patients with dengue with warning signs (DW) or severe dengue (SD). These results significantly improve our understanding of human plasmablast responses in dengue.ImportanceDengue is a globally spreading with over 100 million clinical cases annually with symptoms ranging from mild self-limiting febrile illness to more severe and sometimes life-threatening dengue hemorrhagic fever or shock, especially among children. India contributes nearly a third of global dengue disease burden. The pathophysiology of dengue is complex and remains poorly understood despite many advances indicating a key role for antibody dependent enhancement of infection. While serum antibodies have been extensively studied, the characteristics of the cellular factories responsible for antibody production, i.e., plasmablasts, are only beginning to emerge. This study provides a comprehensive understanding of the magnitude, phenotype, functional and transcriptional profiles of human plasmablasts from dengue patients in India.
- Published
- 2021