Abstract:Objective To investigate the changes in serum YKL-40 level and humoral immune function and their significance in children with recurrent pneumonia. Methods Blood samples were collected from 30 children with recurrent pneumonia (recurrent pneumonia group), 30 children with acute pneumonia (acute pneumonia group), and 30 healthy children (control group). Serum YKL-40 levels were measured by enzyme-linked immunosorbent assay. The correlation between serum YKL-40 level and laboratory indices related to humoral immune function was analyzed. The receiver operating characteristic (ROC) curve was used to analyze the diagnostic value of serum YKL-40 level for recurrent pneumonia. Results The recurrent pneumonia group had a significantly higher serum YKL-40 level than the acute pneumonia and control groups (P < 0.05). The acute pneumonia group had a significantly higher serum YKL-40 level than the control group (P < 0.05). Serum levels of IgG and complement 4 in the recurrent pneumonia group were significantly lower than in the acute pneumonia group (P < 0.05). Serum YKL-40 level was negatively correlated with serum IgG level (rs=-0.309, P=0.047) and serum complement 4 level (r=-0.324, P=0.039). The area under the ROC curve of serum YKL-40 level for diagnosing recurrent pneumonia was 0.958 (95%CI:0.921-0.994). Conclusions Humoral immune function is low in children with recurrent pneumonia. Serum YKL-40 may be involved in the occurrence of recurrent pneumonia and can be used as a reference index for diagnosing recurrent pneumonia.
MA Wei-Yin,PENG Shao,ZHANG Ting. Changes in serum YKL-40 level and humoral immune function and their significance in children with recurrent pneumonia[J]. CJCP, 2017, 19(4): 425-429.
Saad K, Mohamed SA, Metwallety KA. Recurrent/Persistent pneumonia among children in Upper Egypt[J]. Mediterr J Hematol Infect Dis, 2013, 5(1):e2013028.
Owayed AF, Campbell DM, Wang EE. Underlying causes of recurrent pneumonia in children[J]. Arch Pediatr Adolesc Med, 2000, 154(2):190-194.
[6]
Johansen JS, Williamson MK, Rice JS, et al. Identification of proteins secreted by human osteoblastic cells in culture[J]. J Bone Miner Res, 1992, 7(5):501-512.
[7]
Libreros S, Iragavarapu-Charyulu V. YKL-40/CHI3L1 drives inflammation on the road of tumor progression[J]. J Leukoc Biol, 2015, 98(6):931-936.
[8]
Roslind A, Johansen JS. YKL-40:a novel marker shared by chronic inflammation and oncogenic transformation[J]. Methods Mol Biol, 2009, 511(7):159-184.
[9]
Wang HL, Hsiao PC, Tsai HT, et al. Usefulness of plasma YKL-40 in management of community-acquired pneumonia severity in patients[J]. Int J Mol Sci, 2013, 14(11):22817-22825.
[10]
Liu L, Oza S, Hogan D, et al. Global, regional, and national causes of child mortality in 2000-13, with projections to inform post-2015 priorities:an updated systematic analysis[J]. Lancet, 2015, 385(9966):430-440.
[11]
Patria F, Longhi B, Tagliabue C, et al. Clinical profile of recurrent community-acquired pneumonia in children[J]. BMC Pulm Med, 2013, 13:60.
Volck B, Price PA, Johansen JS, et al. YKL-40, a mammalian member of the chitinase family, is a matrix protein of specific granules in human neutrophils[J]. Proc Assoc Am Physicians, 1998, 110(4):351-360.
[14]
Hakala BE, White C, Recklies AD. Human cartilage gp-39, a major secretory product of articular chondrocytes and synovial cells, is a mammalian member of a chitinase protein family[J]. J Biol Chem, 1993, 268(34):25803-25810.
[15]
Malinda KM, Ponce L, Kleinman HK, et al. Gp38k, a protein synthesized by vascular smooth muscle cells, stimulates directional migration of human umbilical vein endothelial cells[J]. Exp Cell Res, 1999, 250(1):168-173.
[16]
Salvatore V, Focaroli S, Teti G, et al. Changes in the gene expression of co-cultured human fibroblast cells and osteosarcoma cells:the role of microenvironment[J]. Oncotarget, 2015, 6(30):28988-28998.
[17]
Senetta R, Duregon E, Sonetto C, et al. YKL-40/c-Met expression in rectal cancer biopsies predicts tumor regression following neoadjuvant chemoradiotherapy:a multi-institutional study[J]. PLoS One, 2015, 10(4):e0123759.
Lee CG, Hartl D, Lee GR, et al. Role of breast regression protein 39(BRP-39)/chitinase 3-like-1 in Th2 and IL-13-induced tissue responses and apoptosis[J]. J Exp Med, 2009, 206(5):1149-1166.
[20]
Letuve S, Kozhich A, Arouche N, et al. YKL-40 is elevated in patients with chronic obstructive pulmonary disease and activates alveolar macrophages[J]. J Immunol, 2008, 181(7):5167-5173.
[21]
Ober C, Tan Z, Sun Y, et a1. Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function[J]. N Engl J Med, 2008, 358(16):1682-1691.
[22]
Tang H, Sun Y, Shi Z, et al. YKL-40 induces IL-8 expression from bronchial epithelium via MAPK (JNK and ERK) and NF-κB pathways, causing bronchial smooth muscle proliferation and migration[J]. J Immunol, 2013, 190(1):438-446.