immunology of infectious and parasitic diseases - XXXVII Congress ...

More documents

Recommendations

Info

EVALUATION OF MACROPHAGE FUNCTION FROM HTLV-1 INFECTED SUBJECTS CAMILA FARIAS AMORIM 1 ; ANSELMO SOUZA 1 ; ANGELA GIUDICE 1 ; SILVANE SANTOS 1 and EDGAR M CARVALHO 1 . 1 Serviço de Imunologia, Complexo Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, Bahia, Brasil. Introduction: The human T lymphotropic virus type 1 (HTLV-1) infection increases susceptibility and worsens the course of other infectious diseases, such as strongyloidiasis and tuberculosis. Since that, it is possible that APCs and/or lymphocytes from HTLV-1 infected individuals have defects in their functions leading to inadequate adaptative immune response against other infectious agent. In this viral infection there is an increased expression of proinflammatory cytokines, and is possible that the constant stimulation of macrophages take these cells to exhaustion. Alternatively, this activation may increase microbicidal ability. Methods and Results: We compared the macrophage function of HTLV-1 carriers (n=13) with soronegative healthy subjects (n=7), evaluating their ability to phagocyte and kill L. braziliensis, analyzing the percentage of infected cells and the number of amastigotes per 100 macrophages. Additionally we determined TNF-, CXCL9 and CXCL10 levels. The percentage of infected cells and the number of amastigotes per 100 cells were quite variable between the two groups studied. There was a trend for lower percentage of infected cells and lower number of amastigotes after 48 and 72 hours infection in cells from HTLV-1 carriers but there was no statistic difference. The TNF-, CXCL9 and CXCL10 levels were higher (p
allow a conclusion about the differences in the killing ability of macrophages from these two groups. Financial support: Instituto Nacional de Ciências e Tecnologia em Doenças Tropicais (INCT-DT) do Ministério de Ciências e Tecnologia (MCT) e o National Institute of Health (NIH).
Page 1 and 2:
IMMUNOLOGY OF INFECTIOUS AND PARASI
Page 3 and 4:
profiles appear to be dependent on
Page 5 and 6:
INVOLVEMENT OF TNF RECEPTORS IN APO
Page 7 and 8:
Effects of bioactive Cryptococcus n
Page 9 and 10:
DCs expressing Indoleamine 2,3-diox
Page 11 and 12:
DETECTION OF GITR ON PATIENT CERVIX
Page 13 and 14:
DETECTION OF GITR AND IL-10 ON CERV
Page 15 and 16:
VACCINATION WITH SM10.3 ANTIGEN, A
Page 17 and 18:
Financial support: FAPESP, CAPES an
Page 19 and 20:
clearance that follows Sylvio X10/4
Page 21 and 22:
EhMSP-1 - AN ENTAMOEBA HISTOLYTICA
Page 23 and 24:
THERAPY WITH SCFV TRANSFECTED-DENDR
Page 25 and 26:
etween the groups. The results show
Page 27 and 28:
Financial support: FIOCRUZ, CNPq.
Page 29 and 30:
elease of NETs from human neutrophi
Page 31 and 32:
ROLE OF CD18 IN ACTIVATION OF M1 MA
Page 33 and 34:
IDENTIFICATION, PURIFICATION AND CH
Page 35 and 36:
with hemin showed higher levels of
Page 37 and 38:
SEPTIC ARTHRITIS TRIGGERED BY S. au
Page 39 and 40:
eing higher levels induced by a vir
Page 41 and 42:
parasite load skin. The TGF-β was
Page 43 and 44:
cultures, both treatments decreased
Page 45 and 46:
observed a tendency to lower parasi
Page 47 and 48:
SERUM COMPONENTS AND MONONUCLEAR CE
Page 49 and 50:
VIABILITY OF LEISHMANIA (L.) CHAGAS
Page 51 and 52:
EVALUATION OF THE INTERFERENCE OF S
Page 53 and 54:
IMMUNODETECTION OF THE TGF- β IN L
Page 55 and 56:
DIFFERENT LEVELS OF NKT AND NK CELL
Page 57 and 58:
Funding: CNPQ; FAPESPA; SESPA; UFPA
Page 59 and 60:
saliva that exacerbated leishmania
Page 61 and 62:
BACTERIAL FILAMENTATION: SUPER-RESI
Page 63 and 64:
IMMUNOLOGICAL PARAMETERS ASSOCIATED
Page 65 and 66: supernatant. BMDC stimulation with
Page 67 and 68: such as number of eosinophils, prot
Page 69 and 70: EVALUATION OF THE PRODUCTION OF TNF
Page 71 and 72: Critical motifs of the Anaplasma ma
Page 73 and 74: SCHISTOSOMA SPP ANTIGENS IMPAIR THE
Page 75 and 76: DOWN-REGULATION OF IFN-g RECEPTOR A
Page 77 and 78: MONOCYTES SUBSETS IN SCHISTOSOMIASI
Page 79 and 80: THE IN VITRO ANALYSIS OF iNOS-KO MO
Page 81 and 82: CCR7 IS CRITICAL FOR RESISTANCE AGA
Page 83 and 84: EVALUATION OF THE IMMUNE RESPONSE A
Page 85 and 86: our data suggest that monocyte secr
Page 87 and 88: DIVERGENT OUTCOMES OF THE INTERACTI
Page 89 and 90: they can deactivate immune effector
Page 91 and 92: Conclusions: We observed a signific
Page 93 and 94: TLR2 AND TLR4 EXPRESSION AND NUTRIT
Page 95 and 96: DEVELOPMENT OF MURINE PLACENTAL MAL
Page 97 and 98: INDUCTION OF TH17 LYMPHOCYTES CONTR
Page 99 and 100: Leishmania amazonensis INCREASES EC
Page 101 and 102: TYPE II GRANULOMA INDUCED BY SCHIST
Page 103 and 104: The Role of Eosinophils in Aspergil
Page 105 and 106: compared to baseline (p
Page 107 and 108: disordered loop and NcSAG2A present
Page 109 and 110: Conclusion: We demonstrate the exis
Page 111 and 112: WT. By contrast, uninfected AhR -/-
Page 113 and 114: in the synthesis of proinflammatory
Page 115: PRODUCTION AND EVALUATION OF CHICKE
Page 119 and 120: contributes to parasite control and
Page 121 and 122: Financial support: FAPESP, CNPq, an
Page 123 and 124: MILTEFOSINE EXERTS ITS LEISHMANICID
Page 125 and 126: IMMUNOMODULATORY ACTIVITIES OF Β-G
Page 127 and 128: REGULATION OF IMMUNE RESPONSE AGAIN
Page 129 and 130: THE ROLE OF REACTIVE OXIGEN SPECIES
Page 131 and 132: INNATE AND ADAPTIVE IMMUNE REPONSE
Page 133 and 134: KINETIC OF THE SPECIFIC HUMMORAL IM
Page 135 and 136: PURINERGIC RECEPTOR P2Y12 ACTIVATIO
Page 137 and 138: Evaluation of cytokine and chemokin
Page 139 and 140: Financial support: This research wa
Page 141 and 142: COMPARISON OF VIRULENCE AND IMMUNE
Page 143 and 144: THE IMPACT OF TUBERCULOSIS IN THE I
Page 145 and 146: GALACTOMANNAN ANTIGENEMIA SCREENING
Page 147 and 148: NATURAL ISOTYPIC RESPONSE AGAINST P
Page 149 and 150: Characterization of costimulatory m
Page 151 and 152: P2X7 RECEPTOR ACTIVATION IS REQUIRE
Page 153 and 154: CASPASE-1 AND NLRP3 CONTRIBUTE TO T
Page 155 and 156: circulating Treg cells expressing C
Page 157 and 158: PBMC, none of the treatments alter
Page 159 and 160: CHARACTERIZATION OF MONOCYTE SUBSET
Page 161 and 162: EFFECT OF OUABAIN IN MACROPHAGES IN
Page 163 and 164: OspC1 AND OspF: VIRULENCE FACTORS I
Page 165 and 166: Conclusion: Taken together, these r
Page 167 and 168:
FIB produced higher proportion of f
Page 169 and 170:
MØ phenotype M2, resulting in decr
Page 171 and 172:
Financial support FAPESP, CAPES, CN
Page 173 and 174:
ALTERATION IN THE DISTRIBUTION OF P
Page 175 and 176:
BENEFICIAL EFFECTS OF PENTOXIFYLLIN
Page 177 and 178:
MODULATION OF IMMUNE RESPONSE AND C
Page 179 and 180:
FAS/FASL AND TRAIL CAUSE APOPTOSIS
Page 181 and 182:
actin were more frequently detected
Page 183 and 184:
NEUTROPHILS AND MACROPHAGES ARE INV
Page 185 and 186:
EXPLORING THE INFLAMMATORY ROLE OF
Page 187 and 188:
CERVICAL LEVELS OF INTERLEUKIN-1 BE
Page 189 and 190:
Title: IDENTIFICATION BY PHAGE DISP
Page 191 and 192:
PROFILE OF PRO- AND ANTI-INFLAMMATO
Page 193 and 194:
IMMUNOMODULATORY MECHANISMS OF SOLU
Page 195 and 196:
EVALUATION OF THE TH1, TH2 AND TH17
Page 197 and 198:
production, as the blockade of PD-L
Page 199 and 200:
CHARACTERIZATION OF POLYMORPHISM TN
Page 201 and 202:
seems to be dependent on M. leprae
Page 203 and 204:
7 with tendency to normalization on
Page 205 and 206:
CHARACTERIZATION OF THE CONSERVATIO
Page 207 and 208:
ASC INFLAMMASOME IS NECESSARY TO AC
Page 209 and 210:
CASPASE-1 IS REQUIRED TO CONTROL OF
Page 211 and 212:
The role of CD4 + T lymphocytes dur
Page 213 and 214:
CRITICAL ROLE OF MYD88 EXPRESSION I
Page 215 and 216:
on ROS, cathepsin B and Syk kinase
Page 217 and 218:
Financial Support: FAPESP and CNPq.
Page 219 and 220:
80% in symptomatic group; 45% in as
Page 221 and 222:
of cells undergoing apoptosis in DT
Page 223 and 224:
Financial support: FAPESP/LIM-56/HC
Page 225 and 226:
identify the active components and
Page 227 and 228:
EVALUATION OF HUMORAL AND CELULLAR
Page 229 and 230:
Financial support: CNPq-PIBIC, FAPE
Page 231 and 232:
addition, significant expression of
Page 233 and 234:
THE ROLE OF K + TRANSPORTERS IN THE
Page 235 and 236:
Conclusion: In this study, we estab
Page 237 and 238:
Heme activates oxidative mechanisms
Page 239 and 240:
ROLE OF ADENOSINE AND PROSTAGLANDIN
Page 241 and 242:
Taken together, our results indicat
Page 243 and 244:
Conclusion: Our findings suggest th
Page 245 and 246:
Financial support: CNPq, CAPES, IOC
Page 247 and 248:
number of circulating parasites in
Page 249 and 250:
CRITICAL ROLE OF IL-6 IN REGULATORY
Page 251 and 252:
PPAR-α AGONIST GEMFIBROZIL DECREAS
Page 253 and 254:
Cutaneous Leishmaniasis in Amazonas
Page 255 and 256:
CYTOTOXICITY IN IMMUNOPATHOGENESIS
Page 257 and 258:
ROS production and TLR2 and 4 expre
Page 259 and 260:
ROLE OF IL-4 IN THE INTESTINAL INFL
Page 261 and 262:
In vitro CULTURE SYSTEM FOR Plasmod
Page 263 and 264:
interactions, Tandem Affinity Purif
Page 265 and 266:
in the course of human infection wi
Page 267 and 268:
findings suggest that IL-17 and IL-
Page 269 and 270:
23 contribute to immunological cont
Page 271 and 272:
not produced during infection by C.
Page 273 and 274:
Conclusion: The production of cytok
Page 275 and 276:
CONCLUSION: It is likely, in this p
Page 277 and 278:
expression in CCC myocardium was 64
Page 279 and 280:
that mononuclear cells derived from
Page 281 and 282:
Conclusion: Altogether, our data sh
Page 283 and 284:
PARACOCCIDIOIDES BRASILIENSIS INHIB
Page 285 and 286:
CANINE VISCERAL LEISHMANIASIS AND S
Page 287 and 288:
IMMUNOMODULATORY EFFECTS OF BIOTHER
Page 289 and 290:
Leishmania EFFECT ON HEME CYTOTOXIC
Page 291 and 292:
ROLE OF STRONGYLOIDES VENEZUELENSIS
Page 293 and 294:
TREATMENT WITH Harpagophytum procum
show all

immunology of infectious and parasitic diseases - XXXVII Congress ...

Create successful ePaper yourself

Delete template?

Save as template?