Table 1. Sequences of primers used for quantitative PCR analysis.

Gene	Forward	Reverse
s18	CCATTCGAACGTCTGCCCTAT	GTCACCCGTGGTCACCATG
il-1α	TTGGTTAAATGACCTGCAACA	GAGCGCTCACGAACAGTTG
il-1β	TGTAATGAAAGACGGCACACC	TCTTCTTTGGGTATTGCTTGG
il-18	CAAACCTTCCAAATCACTTCCT	TCCTTGAAGTTGACGCAAGA
il-1rn	GGCAGTGGAAGACCTTGTGT	CATCTTGCAGGGTCTTTTCC
il-6	GCTACCAAACTGGATATAATCAGGA	CCAGGTAGCTATGGTACTCCAGAA
il-10	CAGAGCCACATGCTCCTAGA	TGTCCAGCTGGTCCTTTGTT
il-12p40	CCATCAGCAGATCATTCTAGACAA	CGCCATTATGATTCAGAGACTG
il-23a	TCCCTACTAGGACTCAGCCAAC	TGGGCATCTGTTGGGTCT
ifnγ	AACTGGCAAAAGGATGGT	GACCTCAAACTTGGCAATAC
ccl2	CATCCACGTGTTGGCTCA	GATCATCTTGCTGGTGAATGAGT
ccl3	TGCCCTTGCTGTTCTTCTCT	GTGGAATCTTCCGGCTGTAG
ccl4	GCCCTCTCTCTCCTCTTGCT	GAGGGTCAGAGCCCATTG
ccl5	TGCAGAGGACTCTGAGACAGC	GAGTGGTGTCCGAGCCATA
ccl11	AGAGCTCCACAGCGCTTCT	GCAGGAAGTTGGGATGGAG
ccl12	CCATCAGTCCTCAGGTATTGG	CTTCCGGACGTGAATCTTCT
cxcl1	TGACAGCGCAGCTCATTG	AGACTCCAGCCACACTCCAA
cxcl9	CTTTTCCTCTTGGGCATCAT	GCATCGTGCATTCCTTATCA
cxcl11	GCTGCTGAGATGAACAGGAA	CCCTGTTTGAACATAAGGAAGC
cxcl12	CTGTGCCCTTCAGATTGTTG	TAATTTCGGGTCAATGCACA