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1 that occurs in Brazil (where VL is caused by L. infantum).
2 us immunity mediated by prior infection with L. infantum.
3 ongipalpis for Leishmania species other than L. infantum.
4 reatment murine model for acute infection by L. infantum.
5  to LdCen(-/-)group following challenge with L. infantum.
6 und 5 showed potent in vivo activity against L. infantum.
7 ld be considered as secondary reservoirs for L. infantum.
8  L. tropica, and 10 have been diagnosed with L. infantum.
9 tropica infection, and 16 were infected with L. infantum.
10                                              L. infantum amastigotes were detected in BM direct smear
11  promastigotes as well as L. amazonensis and L. infantum amastigotes.
12                           Vector-transmitted L. infantum and L. donovani caused >/=5-fold increase in
13                      These data suggest that L. infantum and L. major differentially activate keratin
14 essful development of an SPR sensor for anti-L. infantum antibodies detection in short time, showing
15 nosensor shows good specificity against anti-L. infantum antibodies.
16 % for W2 were obtained for T. cruzi (W1) and L. infantum antigen (W2) samples in three different elec
17 e primary reservoirs of Leishmania infantum (L. infantum), but Leishmania tropica (L. tropica) infect
18 eishmania donovani complex - L. donovani and L. infantum - cause the fatal disease visceral leishmani
19                                  Leishmania (L.) infantum causes visceral, cutaneous, and mucosal lei
20 agasi-containing dermal leukocytes and total L. infantum chagasi parasites in draining lymph nodes we
21 e inoculation site, we introduced metacyclic L. infantum chagasi promastigotes intradermally into BAL
22  the dermis even late after inoculation, and L. infantum chagasi trafficked through neutrophils in bo
23                    From 3 days onward, total L. infantum chagasi-containing dermal leukocytes and tot
24                Nonetheless, a second wave of L. infantum chagasi-containing neutrophils occurred 7 da
25 ere tracked with fluorescent mCherry-labeled L. infantum chagasi.
26 igen (CA), derived from an Iranian strain of L. infantum, compared to direct agglutination test (DAT)
27                                        Thus, L. infantum CYP51 is the first example of a plant-like s
28                                     Although L. infantum CYP51 prefers C4-monomethylated sterol subst
29 nst intracellular amastigotes of Leishmania (L.) infantum evaluated in vitro.
30 microM semipermeable membrane suggested that L. infantum-exposed keratinocytes release soluble factor
31                              By screening an L. infantum expression library with sera from human VL p
32 Long-lasting parasitemia and the presence of L. infantum in bone marrow, revealed that cats could be
33 e immune system function and pathogenesis of L. infantum in cats.
34  10(9) promastigotes of leishmania infantum (L. infantum) in the stationary phase intravenously and s
35         Therefore, our results indicate that L. infantum induces IL-17A production, which promotes th
36                            The prevalence of L. infantum infection in the females fell from 85 to 45%
37 PL-SE induced significant protection against L. infantum infection, with reductions in parasite loads
38 rs were not detected in the initial phase of L. infantum infection.
39                        Only vector-initiated L. infantum infections caused cutaneous lesions at trans
40 was more sensitive than an IFA for detecting L. infantum infections in patients with AIDS.
41 rn Brazilian State of Minas Gerais where L. (L.) infantum is also endemic.
42 range of clinically relevant L. donovani and L. infantum isolates.
43 rates datasets from Leishmania braziliensis, L. infantum, L. major, L. tarentolae, Trypanosoma brucei
44  rK39 in HIV-negative patients infected with L. infantum or L. chagasi declined during treatment with
45 d by confocal microscopy analysis applied to L. infantum promastigotes.
46 roscopy, we have previously identified three L. infantum protein biomarkers (Li-isd1, Li-txn1, and Li
47 sults suggest that TR regions from the novel L. infantum proteins identified in this study are immuno
48 at enhance monocyte control of intracellular L. infantum replication (P < 0.01).
49                 In contrast, the majority of L. infantum samples fell into one globally-distributed g
50                           MDMs infected with L. infantum showed significantly downregulated expressio
51                 Keratinocytes incubated with L. infantum significantly increased expression of proinf
52  (Trypanosoma brucei, Trypanosoma cruzi, and L. infantum) suggests that substrate preferences of plan
53 ochondrial chaperone reservoir, which allows L. infantum to deal successfully with protein unfolding
54 es up to a dilution of 1:10,240 and for anti-L. infantum up to 1:5120 in canine serum samples.
55 s in L. mexicana, L. major, L. donovani, and L. infantum, we demonstrate how this tool can efficientl
56                      The soluble antigens of L. infantum were securely immobilized on an SPR gold dis
57  fly gut populations of both L. mexicana and L. infantum were significantly reduced in caspar-deplete
58 tro activity against the amastigote stage of L. infantum while no activity was observed against proma