grant

The role of neutrophils in the age-driven decline in anti-pneumococcal vaccine responses

Organization STATE UNIVERSITY OF NEW YORK AT BUFFALOLocation AMHERST, UNITED STATESPosted 30 Sept 2021Deadline 31 May 2027
NIHUS FederalResearch GrantFY202565 and older65 or older65 years of age and older65 years of age or more65 years of age or older65+ years65+ years oldAb responseAffectAgeAged 65 and OverAgingAnti-Bacterial AgentsAntibodiesAntibody FormationAntibody ProductionAntibody ResponseAntigen-Presenting CellsAntiseraAutomobile DrivingB blood cellsB cellB cellsB-CellsB-LymphocytesB-cellBacteriaBacterial PneumoniaBindingBlood NeutrophilBlood Polymorphonuclear NeutrophilCD4 CellsCD4 Positive T LymphocytesCD4 T cellsCD4 helper T cellCD4 lymphocyteCD4+ T-LymphocyteCD4-Positive LymphocytesCell BodyCell FunctionCell PhysiologyCell ProcessCellsCellular FunctionCellular PhysiologyCellular ProcessClinicalCo-cultureCocultivationCocultureCoculture TechniquesCommunitiesD pneumoniaeD. pneumoniaeDataDiplococcus pneumoniaeEconomic BurdenElderlyFutureGoalsHealthHost DefenseHost resistanceHumanHuman VolunteersImmuneImmune SeraImmunesImpairmentIn VitroIndividualInfectionInnate Immune ResponseInnate ImmunityLinkMarrow NeutrophilMeasuresMediatingMediatorMemoryMiceMice MammalsMissionModern ManMolecular InteractionMurineMusNative ImmunityNatural ImmunityNeutrophilic GranulocyteNeutrophilic LeukocyteNon-Specific ImmunityNonspecific ImmunityPathway interactionsPhenotypePneumococcal InfectionsPneumococcal conjugate vaccinePneumococcal vaccinePneumococcusPneumoniaPolymorphonuclear CellPolymorphonuclear LeukocytesPolymorphonuclear NeutrophilsPopulationPredispositionPrevenarPrevnarRNA SeqRNA sequencingRNAseqRoleS pneumoniaeS. pneumoniaeShapesSiteStreptococcus pneumoniaeStreptococcus pneumoniae InfectionsStreptococcus pneumoniae vaccineSubcellular ProcessSusceptibilityT cell responseT-CellsT-LymphocyteT4 CellsT4 LymphocytesTestingTimeVaccinatedVaccinationVaccinesWorkabove age 65access to vaccinationaccess to vaccinesaccessory celladaptive immunityadvanced ageafter age 65age 65 and greaterage 65 and olderage 65 or olderageage associated alterationsage associated changesage associated declineage correlated alterationsage correlated changesage dependent alterationsage dependent changesage dependent declineage groupage induced alterationsage induced changesage of 65 years onwardage related alterationsage related changesage related declineage specific alterationsage specific changesagedaged 65 and greateraged 65+aged miceaged mouseaged ≥65agesaging associated alterationsaging associated changesaging correlated alterationsaging correlated changesaging dependent alterationsaging dependent changesaging induced alterationsaging induced changesaging related alterationsaging related changesaging specific alterationsaging specific changesalterations with ageanti-bacterialanti-microbialantibody biosynthesisantimicrobialbacteria pneumoniachanges with ageclinical relevanceclinically relevantcommunity acquired pneumoniacommunity associated pneumoniadecline with agedesigndesigningdetermine efficacydrivingefficacy analysisefficacy assessmentefficacy determinationefficacy evaluationefficacy examinationelderly miceevaluate efficacyexamine efficacygeriatrichealthy aginghealthy human aginghuman old age (65+)immune senescenceimmune serumimmunoglobulin biosynthesisimmunosenescencein vivoinnovateinnovationinnovativemouse modelmurine modelneutrophilnon vaccinatednot vaccinatednovelold miceover 65 yearspathogenpathwaypneumococcal diseasepneumococcus infectionrecruitresponsesenior citizensocial rolethymus derived lymphocytetime usetranscriptome sequencingtranscriptomic sequencingunvaccinatedvaccination accessvaccination availabilityvaccine accessvaccine availabilityvaccine efficacyvaccine responsevaccine responsivenessvaccine-induced response≥65 years
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Full Description

ABSTRACT
Despite the availability of vaccines, Streptococcus pneumoniae (pneumococcus) infections in the elderly

remain a health and economic burden in the USA. This calls for a better understanding of pathways driving

immune dysregulation in aged hosts, reducing vaccine efficacy and rendering this population susceptible to

infections. Our long-term goal is to elucidate the role of polymorphonuclear leukocytes (PMN) in the age-

driven reduction in vaccine responses and increased susceptibility to S. pneumoniae infection. Background:

A key immune cell following S. pneumoniae infection is PMN. PMNs are innate cells required for controlling

bacterial numbers and whose function is known to decline with age. Recent work shows that PMNs are

important regulators of adaptive immunity. However, the role of PMNs in clinically relevant vaccinations and

their impact in the reduced vaccine efficacy seen in aging remains completely unexplored. We found that

vaccination with the pneumococcal conjugate vaccine Prevnar-13, failed to protect old mice against

pneumococcal infection. Further, in young hosts, optimal protection following vaccination required PMNs both

at the time vaccine administration and at the time of pneumococcal-challenge, highlighting the role of PMNs as

both inducers and effectors of vaccine responses. This led to the Hypothesis that age-driven changes in

PMNs result in the decline of vaccine efficacy against S. pneumoniae in the elderly. Here we test this

hypothesis in both murine models and human volunteers with the following Aims: 1) Test the role of PMNs as

effectors in the decline of pneumococcal vaccine efficacy during aging. 2) Test the role of PMNs as inducers of

the age-driven decline in pneumococcal vaccine efficacy. 3) Test the effect of host aging on PMN responses

following vaccination in human donors. Significance/ innovation: Elucidating the role of PMNs in the decline

in vaccine efficacy against pneumococci in the elderly will vastly contribute to our understanding of how aging

alters innate immune responses and how innate immunity in turn regulates the decline in adaptive memory

responses. Further, understanding the role of PMNs, which are involved in host defense against multiple

pathogens, is imperative for future design of better preventative approaches against pneumococci and other

relevant infections that target the vulnerable elderly population. This proposal is perfectly in line with NIA’s

mission to promote healthy aging.

Grant Number: 5R01AG068568-05
NIH Institute/Center: NIH

Principal Investigator: Elsa Bou Ghanem

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