Regulation of B cell Responses in SLE and Other Autoimmune Diseases
Project Number2U19AI110483-11
Former Number3U19AI110483-09
Contact PI/Project LeaderSANZ, IGNACIO E.
Awardee OrganizationEMORY UNIVERSITY
Description
Abstract Text
The overarching objective of the Emory Autoimmunity Center of Excellence (ACE) U19 is to
decipher the molecular programs responsible for the aberrant B cell responses underpinning
autoimmune diseases. A central tenet of the Emory ACE is that unraveling the heterogeneity
of human autoimmune diseases and translating that knowledge into mechanistically based
treatments requires an integrated collaboration between physician-scientists, basic scientists,
and expert clinicians with access to large populations of well-characterized autoimmune
patients. Our fundamental goals are: (1) to understand B cell dysregulation in SLE using single
cell interrogation of their molecular roadmaps, and (2) to assemble a scientific and
technological platform that engages other ACE U19 and UM1 Centers through the
Collaborative Project to perform similar studies in other immune cells and autoimmune
disorders. These goals will be realized through a highly integrated collaboration between the
three components of the Scientific Program supported by an Administrative Core. In the
Principal Project, Dr. Sanz will ascertain the heterogeneity of effector B cells, their regulatory
programs, and their differential utilization according to disease endotypes, and investigate the
diversity and regulation of SLE memory cells. Specifically, his group will analyze germinal
center dependent and independent memory and the role of antigenic persistence in the
regulation of autoimmune and protective memory. In the Collaborative Project, Dr. Boss will
investigate the epigenetic regulation of B cells and other immune cells in SLE and other human
autoimmune diseases as part of the Collaborative Agenda that will be developed within the
new ACE centers. Finally, in the Pilot Project, Dr. Scharer will pursue the functional
characterization of SLE B cell differentiation using high-throughput loss-of-function and gain-of-
function CRISPR screens. The Emory ACE also proposes to continue to manage the ACE
Funds Management Core and to establish a centralized ACE Biorepository Core to coordinate
the collection, storage, and management of samples from the Emory ACE and ACE Clinical
Projects and their allocation for use in mechanistic studies. Collectively, the work proposed
should contribute greatly to the charter mission and goals of the Autoimmunity Centers of
Excellence Network.
Public Health Relevance Statement
Human autoimmune diseases comprise a large number of conditions including systemic diseases
such as Lupus or Rheumatoid Arthritis and organ-specific diseases such as Type 1 Diabetes and
Multiple Sclerosis. To understand this complexity, there is a need to continue the multidisciplinary
work that has been fostered by the Autoimmunity Centers of Excellence Network over the last 25
years. The Emory Autoimmunity Center of Excellence will continue our work in Lupus while
collaborating with other ACE Centers in the study of other autoimmune diseases.
NIH Spending Category
No NIH Spending Category available.
Project Terms
Administrative CoordinationAntigensAutoantigensAutoimmuneAutoimmune DiseasesAutoimmune ResponsesAutoimmunityB cell differentiationB-LymphocytesCRISPR screenCell PhysiologyCellsClinicalClinical ProtocolsClinical ResearchCollaborationsCollectionDiagnosisDiseaseEpigenetic ProcessFosteringFundingGenerationsGenesGenetic Predisposition to DiseaseGoalsHeterogeneityHumanImmuneImmunoglobulin-Secreting CellsImmunologicsIndividualInsulin-Dependent Diabetes MellitusKnowledgeLeadershipLupusMemoryMemory B-LymphocyteMissionMolecularMultiple SclerosisOrganPathogenicityPathway interactionsPatientsPhysiciansPilot ProjectsPlayPopulationProcessRegulationResearchResourcesRheumatoid ArthritisRoleSamplingScientistStructure of germinal center of lymph nodeSystemic Lupus ErythematosusSystemic diseaseTechnologyTranslatingUniversitiesWorkbiobankclinical developmentepigenetic regulationexperiencegain of functionimmunogenicinnovationloss of functionmembermultidisciplinarynoveloperationprogramsresponsetechnology platform
National Institute of Allergy and Infectious Diseases
CFDA Code
855
DUNS Number
066469933
UEI
S352L5PJLMP8
Project Start Date
01-May-2014
Project End Date
30-April-2029
Budget Start Date
08-May-2024
Budget End Date
30-April-2025
Project Funding Information for 2024
Total Funding
$4,394,852
Direct Costs
$3,844,798
Indirect Costs
$550,054
Year
Funding IC
FY Total Cost by IC
2024
National Institute of Allergy and Infectious Diseases
$4,279,748
2024
NIH Office of the Director
$115,104
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 2U19AI110483-11
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
No Publications available for 2U19AI110483-11
Patents
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Outcomes
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No Outcomes available for 2U19AI110483-11
Clinical Studies
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News and More
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History
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Similar Projects
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