ライフサイエンスコーパス: infantum

1 es in the host immune response to Leishmania infantum.

2 immunity mediated by prior infection with L. infantum.

3 n against visceral infection with Leishmania infantum.

4 irst linked to the clinical syndrome roseola infantum.

5 tment murine model for acute infection by L. infantum.

6 14alpha-demethylase (CYP51) from Leishmania infantum.

7 eral leishmaniasis (VL) caused by Leishmania infantum.

8 tabase of the parasitic protozoan Leishmania infantum.

9 murine infection model employing Leishmania infantum.

10 positive patients coinfected with Leishmania infantum.

11 pesvirus 6 is the causative agent of roseola infantum, a generally benign rash illness of infants.

12 iasis is caused by infection with Leishmania infantum, a Protist parasite transmitted by blood-feedin

13 omastigotes as well as L. amazonensis and L. infantum amastigotes.

14 ed tandem repeat (TR) proteins of Leishmania infantum and an evaluation of VL patient antibody respon

15 Vector-transmitted L. infantum and L. donovani caused >/=5-fold increase in sp

16 These data suggest that L. infantum and L. major differentially activate keratinocy

17 mes of two species of Leishmania: Leishmania infantum and Leishmania braziliensis.

18 ies of Leishmania, L. tarentolae, Leishmania infantum, and L. major, produced hypersensitivity to bot

19 ful development of an SPR sensor for anti-L. infantum antibodies detection in short time, showing a g

20 ensor shows good specificity against anti-L. infantum antibodies.

21 or chip for the detection of anti-Leishmania infantum antibodies.

22 gly indicate that hamsters infected with Le. infantum become significantly more attractive to a great

23 ntly, this analysis suggests that Leishmania infantum chagasi alters the expression profile of certai

24 The vector-borne protozoan Leishmania infantum chagasi causes minimal inflammation after inocu

25 si-containing dermal leukocytes and total L. infantum chagasi parasites in draining lymph nodes were

26 noculation site, we introduced metacyclic L. infantum chagasi promastigotes intradermally into BALB/c

27 Metacyclic Leishmania infantum chagasi promastigotes were treated with methyl-

28 n abundance during development of Leishmania infantum chagasi to a virulent metacyclic stage, as did

29 e dermis even late after inoculation, and L. infantum chagasi trafficked through neutrophils in both

30 role of HO-1 in the infection by Leishmania infantum chagasi, the causative agent of VL cases in Bra

31 From 3 days onward, total L. infantum chagasi-containing dermal leukocytes and total

32 Nonetheless, a second wave of L. infantum chagasi-containing neutrophils occurred 7 days

33 caused by Leishmania donovani and Leishmania infantum chagasi.

34 tracked with fluorescent mCherry-labeled L. infantum chagasi.

35 th in the presence and absence of Leishmania infantum chagasi.

36 lpis sand flies, known vectors of Leishmania infantum/chagasi parasites, in a Brazilian city endemic

37 oplasma gondii, Neospora caninum, Leishmania infantum, Cryptosporidium parvum, or canine DNA under an

38 Thus, L. infantum CYP51 is the first example of a plant-like ster

39 Although L. infantum CYP51 prefers C4-monomethylated sterol substrat

40 ination experiments employing the Leishmania infantum D-13 (p80) antigen, significantly higher levels

41 L. major and a visceral strain of Leishmania infantum, each bearing a different drug-resistant marker

42 roM semipermeable membrane suggested that L. infantum-exposed keratinocytes release soluble factors t

43 By screening an L. infantum expression library with sera from human VL pati

44 2.5 mg/kg (b.i.d., orally) in the Leishmania infantum hamster model.

45 a protein of unknown function in Leishmania infantum (hypothetical C1 protein) and specific antibodi

46 ethods for molecular detection of Leishmania infantum in the canine reservoir host.

47 apeutic strategies for control of Leishmania infantum in this important reservoir species.

48 agent of zoonotic leishmaniasis, Leishmania infantum, in France and Iberia, and provides a rare case

49 Therefore, our results indicate that L. infantum induces IL-17A production, which promotes the c

50 Leishmania infantum-infected dogs are a naturally occurring model o

51 imental vector transmissions with Leishmania infantum-infected Lutzomyia longipalpis.

52 The prevalence of L. infantum infection in the females fell from 85 to 45%.

53 Control of Leishmania infantum infection is dependent upon Th1 CD4(+) T cells

54 SE induced significant protection against L. infantum infection, with reductions in parasite loads of

55 related to the protection against Leishmania infantum infection.

56 Only vector-initiated L. infantum infections caused cutaneous lesions at transmis

57 more sensitive than an IFA for detecting L. infantum infections in patients with AIDS.

58 razilian State of Minas Gerais where L. (L.) infantum is also endemic.

59 es datasets from Leishmania braziliensis, L. infantum, L. major, L. tarentolae, Trypanosoma brucei an

60 15 were screened in vitro against Leishmania infantum , Leishmania braziliensis , Leishmania guyanens

61 e vector-borne protozoan parasite Leishmania infantum, mitochondrial peroxiredoxin (Prx) exerts intri

62 s sorted on contact with visceral Leishmania infantum on a susceptible mice model evaluating the subs

63 ave been recently developed using Leishmania infantum or Chikungunya virus (CHIKV).

64 39 in HIV-negative patients infected with L. infantum or L. chagasi declined during treatment with me

65 Lutzomyia longipalpis to transmit Leishmania infantum or Leishmania donovani to hamsters.

66 rtalized human keratinocytes with Leishmania infantum or Leishmania major, which cause visceral or cu

67 y confocal microscopy analysis applied to L. infantum promastigotes.

68 ts suggest that TR regions from the novel L. infantum proteins identified in this study are immunodom

69 enhance monocyte control of intracellular L. infantum replication (P < 0.01).

70 Keratinocytes incubated with L. infantum significantly increased expression of proinflam

71 rypanosoma brucei, Trypanosoma cruzi, and L. infantum) suggests that substrate preferences of plant-

72 ations of the medically important Leishmania infantum (syn.

73 ondrial chaperone reservoir, which allows L. infantum to deal successfully with protein unfolding con

74 if the odour of hamsters, infected with Le. infantum, was more attractive than the odour of the same

75 ruzi, Leishmania braziliensis and Leishmania infantum were not clinically relevant.

76 The soluble antigens of L. infantum were securely immobilized on an SPR gold disk b

77 y gut populations of both L. mexicana and L. infantum were significantly reduced in caspar-depleted f

78 Transfection of Leishmania infantum with LmACR2 augmented Pentostam sensitivity in