PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
25567153-16	2014	CONCLUSIONS: Losartan has a protective effect on LPS-induced ALI, which may be partly dependent on suppressions of Th1 and Th17 polarization response.	Losartan	13-21	negative elongation factor complex member C/D, Th1l	Mus musculus	115-118	
22020765-0	2012	Losartan inhibits conventional dendritic cell maturation and Th1 and             Th17 polarization responses: Nuovel mechanisms of preventive effects on lipopolysaccharide-induced             acute lung injury.	Losartan	0-8	negative elongation factor complex member C/D, Th1l	Mus musculus	61-64	
22020765-8	2012	In addition, polarized Th1 and Th17 responses were markedly increased in LPS-induced ALI mice at 24 and 48 h. Of note, losartan led to inhibition of respiratory cDCs maturation at 6 h and suppressed Th1 and Th17 polarization responses compared with ALI mice at 24 and 48 h. Collectively, our findings may provide a novel and, at least, partial explanation for the protective effects by which losartan inhibits lung cDCs maturation and suppresses Th1 and Th17 immune responses.	Losartan	119-127	negative elongation factor complex member C/D, Th1l	Mus musculus	23-26	
22020765-8	2012	In addition, polarized Th1 and Th17 responses were markedly increased in LPS-induced ALI mice at 24 and 48 h. Of note, losartan led to inhibition of respiratory cDCs maturation at 6 h and suppressed Th1 and Th17 polarization responses compared with ALI mice at 24 and 48 h. Collectively, our findings may provide a novel and, at least, partial explanation for the protective effects by which losartan inhibits lung cDCs maturation and suppresses Th1 and Th17 immune responses.	Losartan	119-127	negative elongation factor complex member C/D, Th1l	Mus musculus	31-34	
22020765-8	2012	In addition, polarized Th1 and Th17 responses were markedly increased in LPS-induced ALI mice at 24 and 48 h. Of note, losartan led to inhibition of respiratory cDCs maturation at 6 h and suppressed Th1 and Th17 polarization responses compared with ALI mice at 24 and 48 h. Collectively, our findings may provide a novel and, at least, partial explanation for the protective effects by which losartan inhibits lung cDCs maturation and suppresses Th1 and Th17 immune responses.	Losartan	119-127	negative elongation factor complex member C/D, Th1l	Mus musculus	31-34