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1 ease globally in parallel with a decrease in parasitic infection.
2 omponents of the innate immune system during parasitic infection.
3 egral link in the chronic immune response to parasitic infection.
4 e important in Th2 cell-mediated immunity to parasitic infection.
5 tripartite model for nematode parasitism and parasitic infection.
6 beta induction and other markers of viral or parasitic infection.
7 the CD8(+) T cells during both a viral and a parasitic infection.
8 -49 receptor-expressing NK cell subsets in a parasitic infection.
9 -helper cells may be modulated by concurrent parasitic infection.
10 arthenogenetic Daphnia magna with respect to parasitic infection.
11 diated immune responses for an intracellular parasitic infection.
12 facilitate recognition and treatment of this parasitic infection.
13 tic doses to animals to selectively arrest a parasitic infection.
14 tion of the IgE response to allergens and to parasitic infection.
15 kk-1) upon allergen challenge or non-healing parasitic infection.
16 allergic inflammation and protection against parasitic infection.
17 the liver that can determine the outcome of parasitic infection.
18 igher background rate of eosinophilia due to parasitic infection.
19 expression was up-regulated in response to a parasitic infection.
20 to humans and an important blood-borne human parasitic infection.
21 the drug discovery pipeline for this deadly parasitic infection.
22 uring Th2-mediated immune responses, such as parasitic infections.
23 llular infiltrate associated with asthma and parasitic infections.
24 ty-adjusted life year (DALY), is unsuited to parasitic infections.
25 reatment of cancer, heart disease, AIDS, and parasitic infections.
26 both human and veterinary medicine to treat parasitic infections.
27 reatment of cancer, heart disease, AIDS, and parasitic infections.
28 tokine production and protective immunity to parasitic infections.
29 in parasite epidemiology and the control of parasitic infections.
30 therapeutics for the treatment of cancer and parasitic infections.
31 plain many immune features characteristic of parasitic infections.
32 n allergic diseases and the host response to parasitic infections.
33 model for the study of human and veterinary parasitic infections.
34 novel drug targets and vaccine candidates in parasitic infections.
35 tion of eosinophils in allergic diseases and parasitic infections.
36 eripheral blood T cells during bacterial and parasitic infections.
37 ment of eosinophils in allergic diseases and parasitic infections.
38 e and may confer physiological protection in parasitic infections.
39 cancers associated with bacterial, viral, or parasitic infections.
40 an attractive drug target for the control of parasitic infections.
41 diated disorders such as allergy, atopy, and parasitic infections.
42 in the initial suppression of bacterial and parasitic infections.
43 kers, is a common occurrence in HIV and some parasitic infections.
44 eactive protein levels and low prevalence of parasitic infections.
45 rfusion injury, enteroinvasive bacterial and parasitic infections.
46 s a possible source for symptom disparity in parasitic infections.
47 lt in flare-ups of many bacterial, viral and parasitic infections.
48 ron metabolism and the etiology of anemia in parasitic infections.
49 odulatory functions in allergic diseases and parasitic infections.
50 mmune responses during viral, bacterial, and parasitic infections.
51 n diverse diseases from cancer to eukaryotic parasitic infections.
52 rological diseases and disorders, as well as parasitic infections.
53 including aggressive cancer, arthritis, and parasitic infections.
54 region occurred for select diagnoses such as parasitic infections.
55 eir contribution to enhance host exposure to parasitic infections.
56 ify new treatments for asthma, allergies and parasitic infections.
57 with high peanut consumption and widespread parasitic infections.
58 skin reactivity), consumption patterns, and parasitic infections.
59 ses, IL-17E is essential for defense against parasitic infections.
60 reatment of cancer, heart disease, AIDs, and parasitic infections.
61 ulating intracellular bacterial, fungal, and parasitic infections.
62 herpes viruses, mycobacteria, and fungal and parasitic infections, a single arm of the immune respons
63 in the past year fatal viral, fungal, and/or parasitic infections accounted for 16% and 34% of the mo
64 ted for centuries as chronically disfiguring parasitic infections affecting millions of people across
65 ory states arising from viral, bacterial and parasitic infection, allergic and asthmatic reactions, a
66 The pathological process was recognised as a parasitic infection, although its features were differen
69 response able to clear bacterial, viral, and parasitic infection and an ability to efficiently store
70 ation of IFN-gamma-mediated immunity to this parasitic infection and identify a novel function for th
72 complexity of the murine host response to a parasitic infection and suggest that an outbred human po
73 rinary and human medicine for the control of parasitic infection and was the joint focus of the 2015
74 s that regulate both protective responses in parasitic infections and allergic airway inflammation.
78 icle, we review the current understanding of parasitic infections and basophils and discuss their put
82 4-dependent, Th2-mediated responses in other parasitic infections and in models of allergic asthma, t
83 reports on the exact roles for IL-17 during parasitic infections and limited knowledge about cellula
85 This approach may find useful application in parasitic infections and more broadly in any disease sta
87 rnivore scavenging strategies under risks of parasitic infection, and (iii) conducting a literature-r
89 te that CD4+ TRM cells form in response to a parasitic infection, and indicate that optimal protectiv
90 ied a novel inhibitory function for IL-17 in parasitic infection, and our results demonstrate importa
91 52 days) elapsed before the first documented parasitic infection, and the median intervals from arriv
92 y recruited into the CNS in response to this parasitic infection, and they were able to target the in
93 g, 34 serum samples from patients with other parasitic infections, and 15 normal human serum samples.
95 ector functions during bacterial, viral, and parasitic infections, and contributed to innate response
96 admission included malnutrition and wasting, parasitic infections, and haematological disorders in th
97 eptors have not been investigated to date in parasitic infections, and little is known about the role
98 loped because they are already used to treat parasitic infections, and there is interest in their use
100 tion of drugs against bacterial, fungal, and parasitic infections, antineoplastic agents against canc
101 The pathological processes resulting from parasitic infection are known to have important impacts
107 capable of preventing viral, bacterial, and parasitic infections are currently under development.
109 better management of malaria and intestinal parasitic infections are likely to reduce the incidence
112 s review focuses on studies that use enteral parasitic infections as a tool to investigate the functi
113 ignature appear during viral, bacterial, and parasitic infections, but also arise during humoral auto
114 number of enteric infections, including many parasitic infections, but also likely provide protection
118 Schistosomiasis or snail fever is an endemic parasitic infection caused by various trematodes of the
119 nological rationale underpinning therapeutic parasitic infection, describe recently initiated trials,
120 atopoietic growth factors or emerging during parasitic infections, display tolerogenic properties.
121 effect of stunting, diarrhoeal disease, and parasitic infections during infancy on cognitive functio
122 incidence and natural history of intestinal parasitic infections during the PCVs' >2-year overseas s
123 mass drug administration (MDA) against these parasitic infections emphasise treatment of school-aged
128 ective innate immunity against bacterial and parasitic infections; however, its role in host immunity
129 adpoles leads to increased susceptibility to parasitic infection in adult frogs, in the absence of su
131 rovide possible explanations for the role of parasitic infection in susceptibility and resistance to
138 across age, sex, anthropometric indexes, and parasitic infections in a representative sample of 3595
139 chronic infection is one of the most common parasitic infections in humans and can be reactivated to
141 T cell differentiation and susceptibility to parasitic infections in murine models, we compared T cel
142 tervention addressing 2 of the most virulent parasitic infections in pregnant women in sub-Saharan Af
143 osomiasis are the world's two most important parasitic infections in terms of distribution, morbidity
144 risk of common bacterial, viral, fungal, and parasitic infections in the general population of indivi
146 tudies toxoplasmosis, one of the most common parasitic infections in the world, caused by Toxoplasma
148 at can protect against bacterial, viral, and parasitic infections, including lethal influenza and mal
149 th a broad-spectrum activity against various parasitic infections, including malaria, toxoplasmosis a
150 vaccines are available for human use for any parasitic infections, including the helminthic disease s
152 o Leishmania major (Lm) or Toxoplasma gondii parasitic infections, indicating that exogenously delive
153 The direct benefit to females of avoiding parasitic infection is proposed to lead to the linkage b
160 s and those chronic and debilitating (mostly parasitic) infections known as neglected tropical diseas
161 d neoplastic (chronic lymphocytic leukemia), parasitic infection (Leishmania major), and infectious d
163 This review discusses T cell exhaustion in parasitic infection, mechanisms of development, and a po
165 r regulation of immune responses, such as in parasitic infection, necessitate further characterizatio
170 tion problems, particularly the influence of parasitic infections on child health and nutrition.
171 munity that can either be protective against parasitic infection or cause tissue damage in allergy an
172 patients affected by Th2 pathologies such as parasitic infections or atopic dermatitis often suffer f
175 esults are negative, O&P can be performed if parasitic infections other than G. lamblia, E. histolyti
176 ietary factors such as chronic inflammation, parasitic infections, overweight, and genetic hemoglobin
177 l established risk factors for CC, including parasitic infections, primary sclerosing cholangitis, bi
178 sed by granulomatous disorders, DNA viruses, parasitic infections, pulmonary amyloidosis, vascular ca
179 ationship was mostly explained by fungal and parasitic infections rather than by viral and bacterial
183 wever, the role of NK cells in extracellular parasitic infections such as filarial infections is not
188 l burden of high E4 prevalence combined with parasitic infections that can also reduce cognitive perf
189 e habitat for intermediate hosts of tropical parasitic infections that cause disease and suffering.
190 e been proposed by which hosts can withstand parasitic infections, the role of multiple infections an
191 rheal episodes, the continued acquisition of parasitic infections throughout the PCVs' >2-year stay i
192 rol patients who had other parasitic and non-parasitic infections to a weak cation exchange chip, and
196 lations with a high prevalence of intestinal parasitic infections, two independently collected stool
197 d mortality associated with these intestinal parasitic infections warrant the development of rapid an
198 ed modelling showed that only positivity for parasitic infections was a significant predictor of redu
200 dazole, an oral drug currently used to treat parasitic infections, was used as a positive control.
202 n thus offers an example of an intracellular parasitic infection where CD8(+) T-cell immunity can be
203 s suggests an innate immune response against parasitic infections, whereas the other gene expression
204 r without Schistosoma mansoni coinfection, a parasitic infection with T helper (Th) 2 immune bias.
206 The physiological effects of such events on parasitic infections within endotherms are poorly studie
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