Immunophenotyping and Transcriptional Profiling of Human Plasmablasts in Dengue.
Charu AggarwalKeshav SainiElluri Seetharami ReddyMohit SinglaKaustuv NayakYadya M ChawlaDeepti MaheshwariPrabhat SinghPragati SharmaPriya BhatnagarSanjeev KumarKamalvishnu GottimukkalaHarekrushna PandaSivaram GunisettyCarl W DavisHaydn Thomas KissickSushil Kumar KabraRakesh LodhaGuruprasad R MedigeshiRafi AhmedKaja Murali-KrishnaAnmol ChandelePublished in: Journal of virology (2021)
Plasmablasts represent a specialized class of antibody-secreting effector B cells that transiently appear in blood circulation following infection or vaccination. The expansion of these cells generally tends to be massive in patients with systemic infections such as dengue or Ebola that cause hemorrhagic fever. To gain a detailed understanding of human plasmablast responses beyond antibody expression, here, we performed immunophenotyping and RNA sequencing (RNA-seq) analysis of the plasmablasts from dengue febrile children in India. We found that plasmablasts expressed several adhesion molecules and chemokines or chemokine receptors that are involved in endothelial interactions or homing to inflamed tissues, including skin, mucosa, and intestine, and upregulated the expression of several cytokine genes that are involved in leukocyte extravasation and angiogenesis. These plasmablasts also upregulated the expression of receptors for several B-cell prosurvival cytokines that are known to be induced robustly in systemic viral infections such as dengue, some of which generally tend to be relatively higher in patients manifesting hemorrhage and/or shock than in patients with mild febrile infection. These findings improve our understanding of human plasmablast responses during the acute febrile phase of systemic dengue infection. IMPORTANCE Dengue is 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. 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 early cellular factories responsible for antibody production, i.e., plasmablasts, are only beginning to emerge. This study provides a comprehensive understanding of the transcriptional profiles of human plasmablasts from dengue patients.
Keyphrases
- zika virus
- aedes aegypti
- dengue virus
- endothelial cells
- rna seq
- single cell
- end stage renal disease
- poor prognosis
- high glucose
- induced pluripotent stem cells
- ejection fraction
- chronic kidney disease
- pluripotent stem cells
- young adults
- gene expression
- prognostic factors
- newly diagnosed
- staphylococcus aureus
- escherichia coli
- urinary tract infection
- early onset
- sars cov
- immune response
- patient reported outcomes
- multidrug resistant
- cystic fibrosis
- depressive symptoms
- regulatory t cells
- cell proliferation
- vascular endothelial growth factor
- long non coding rna
- candida albicans
- chemotherapy induced
- cell migration