- Open Access
Anti-erythropoietin antibody levels and its association with anaemia in different strains of semi-immune mice infected with Plasmodium berghei ANKA
© Helegbe et al.; licensee BioMed Central Ltd. 2013
- Received: 27 April 2013
- Accepted: 19 August 2013
- Published: 27 August 2013
Malaria anaemia is still a major public health problem and its pathogenesis still unclear. Interestingly, the progression of anaemia is at relatively low parasitaemia with some mortality in the semi-immune individuals in the endemic areas despite adequate erythropoietin (EPO) synthesis. A recent study has shown that treatment with exogenous anti-erythropoietin (anti-EPO) antibodies (Ab) of infected mice gives protection against malaria infection, suggesting an important role for anti-EPO Ab in malaria. The objective of the study was to evaluate anti-EPO antibody levels in anaemic condition of different strains of semi-immune mice with malaria.
Semi-immune status was attained in four mice strains (Balb/c, B6, CBA and NZW) by repeated infections with 104Plasmodium berghei ANKA, and treatment with chloroquine/pyrimethamine. ELISA was used to measure anti-EPO Ab, transferrin and EPO while inflammatory cytokines measurement was done using bead-based multiplex assay kit.
The mean anti-EPO Ab levels in the mice strains [Optical Density (OD) values at 450 nm: Balb/c (2.1); B6 (1.3); CBA (1.4) and NZW (1.7)] differed (p = 0.045), and were significantly higher when compared with uninfected controls, p < 0.0001, and mean anti-EPO Ab levels in the mice strains at recovery [OD values at 450 nm: Balb/c (1.8); B6 (1.1); CBA (1.5) and NZW (1.0) also differed (p = 0.0004). Interestingly, EPO levels were significantly high in NZW and low in Balb/c mice (p < 0.05), with those of B6 and CBA of intermediary values. Again, NZW were highly parasitaemic (20.7%) and the other strains (Balb/c, B6 and CBA) ranged between 2.2-2.8% (p = 0.015). Anti-EPO Ab correlated positively with extent of Hb loss (r = 0.5861; p = 0.003). Correlation of anti-EPO antibody with EPO was significant only in Balb/c mice (r = −0.83; p = 0.01). Significant levels of IL6 and IFNγ (p < 0.0001), both known to be associated with erythropoiesis suppression were observed in the Balb/c. Transferrin was significantly lower in Balb/c (p < 0.0001) when compared with the other mice strains (B6, CBA and NZW).
This is the first ever report in estimating endogenous anti-EPO antibodies in malaria anaemia. The data presented here suggest that anti-EPO Ab is produced at infection and is associated with Hb loss. Host factors appear to influence anti-EPO antibody levels in the different strains of mice.
- Anti-EPO antibody
- Malaria anaemia
- Plasmodium berghei ANKA
- Semi immune
Malarial infections result in a significant destruction of both infected red blood cells (iRBC) and uninfected red blood cells. It has been observed in chronic infected individuals or in the semi-immune, that the anaemia reported does not correlate with the level of parasitaemia[1, 2]. Possible mechanisms that have been suggested are defective production of RBC or an excessive rate of red cells destruction or a combination of both[3, 4]. However, studies have shown that erythropoietin (EPO) level is adequate in infected children and experimental models[5–7], and thus it is surprising that anaemia is not improved in that measure. Erythropoietin (EPO), a glycoprotein hormone, being a cytokine controls erythropoiesis or red blood cell production.
Studies in some auto-immune diseases and HIV patients revealed high level of anti-EPO auto-antibodies and its association with anaemia[8–10]. But this has not been studied in malaria anaemia cases. The use of EPO in therapy has been recommended to alleviate anaemia due to malarial infections and also in cerebral malaria management. The suggestion is that use of EPO will help a great deal in minimizing the risk of HIV/AIDS via blood transfusion when not screened properly. Meanwhile, EPO has been used successfully in a couple of diseases, treating anaemia in AIDS, in renal failure, as well as for limiting brain damage in experimental auto-immune encephalomyelitis, and also been proposed for treatment of haemoglobinopathies in which β-globin synthesis is affected[16, 17]. These suggest an important role for EPO in therapy. However, neutralizing IgG antibodies to the protein component of exogenous recombinant EPO are found to cross-react with endogenous erythropoietin. Thus, the question that remains to be clarified is whether antibodies are produced against endogenous EPO and what the implications are during Plasmodium infections.
High level of anti-EPO auto-antibodies has been observed in some auto-immune diseases, but not reported in malaria anaemia (which has been thought to be auto-immune mediated). As a result anti-EPO antibodies may be implicated in malaria anaemia cases. Therefore, a study evaluating the levels of anti-EPO antibodies in malaria anaemia will be of interest to assess the benefits and/or predict (un)expected complications that may arise in the administration of exogenous EPO as therapeutic measure in malaria anaemia cases. Related to that, induction of antibodies against EPO molecule was observed in patients treated with recombinant human EPO which resulted in pure red cell aplasia. Furthermore, the use of anti-EPO auto-antibodies as a therapy in murine malaria studies, is an indication of the important role it may play in severe malaria anaemia.
A previous study has shown that one mechanism of anaemia during Plasmodium infection was the destruction of uninfected red blood cells. The current study aims to describe an alternative mechanism of anaemia by using sera raised from this previous study. Thus, the level of anti-EPO antibodies in malaria anaemia situation of different strains of semi-immune mice was evaluated. Furthermore, to investigate if host factors may play a role, different strains of semi-immune mice were used.
Mice, infection and generation of semi-immune status
The study was conducted strictly according to the recommendation in the Fundamental Guidelines for Proper Conduct of Animal Experiment and Related Activities in Academic Research Institutions under the jurisdiction of the Ministry of Education, Culture, Sports, Science and Technology, Japan (Notice no. 71). All animal experiments were approved by the Nagasaki University, Board of Animal Research, according to Japanese Guideline for use of experimental animals (Permit Number 0811130716). All efforts were made to humanely minimize animal suffering.
Screening of sera for anti-EPO antibodies by immunodot blot
Ultrabind US450 membrane (Gelman Sciences, Japan) was cut according to size and pre-wet with enough volume of tris-buffered saline (TBS). The membrane was placed unto the manifold and 300 μL TBS used to wash wells and membranes. Recombinant mouse EPO (R&D Systems, Japan, Catalogue Number 959-ME) was used as antigen to coat the membrane overnight at 4°C. The membrane in each well was blocked with 100 μL BlockAce (Catalogue No. UK-B25, Dainippon Pharmaceutical Co. Osaka, Japan) for an hour. Membranes in the wells were later washed once with 300 μL tris-buffered saline with tween (TTBS). Primary antibody (from infected sera and uninfected mice sera as negative control) were diluted at 1:10, 1:20 and incubated with the mouse EPO antigen for 3 hours at RT. The membranes in the wells were washed with 300 μL of TTBS twice before they were finally removed from the manifold and washed once in TTBS on a rotating machine. Secondary antibody of goat anti-mouse IgG-conjugated horse-radish peroxidase (HRP) at 1:2,000 dilution was incubated with the membrane for an hour at room temperature (RT) in the dark. Membrane was washed four times with TTBS and once with TBS to remove residual TTBS from membrane. Color development was done by addition of diaminobenzidine (DAB, at 5.0 mg/10 ml PBS + 5 uL H202) and incubated at RT for 10–15 min.
Measurement of anti-EPO antibodies
This was done based on modified method according to Tzioufas et al.. The recombinant mouse EPO (R&D Systems, Japan, Catologue Number 959-ME) was used as antigen. It was dissolved in phosphate buffered saline (PBS, pH 7.2), and coated in the polystyrene micro titer plate at 0.09 μg per well. After incubation overnight at 4°C, plates were washed with 0.1% Tween 20/PBS and blocking was done with Block Ace (Catalogue No. UK-B25, Dainippon Pharmaceutical Co. Osaka, Japan) for 1 hour. Diluted serum samples from the infected mice and uninfected mice (serving as negative control) all at 1:1,000 dilutions was added to the wells in duplicate and incubated for three hours at 37°C. After washing for five times with 0.1% Tween 20/PBS, 100 μL horse radish peroxidase (HRP)-conjugated goat anti-mouse IgG (Catalogue number 55563, MP Biomedicals, LLC 29525 Fountain Pkwy Solon, OH 44139, USA) at 1:2,500 was added to the wells in the 96-well ELISA plates and incubated for an hour at RT. Washing was done five times with 0.1% Tween 20/PBS and reaction visualized by the addition of 100 μL stabilized chromogen (Part/Lot number SS01/302008, Biosource, Carmarillo, CA, USA). Reaction was stopped 20 minutes later by the addition of 50 μL 1 N H2SO4 and absorbance was measured in the ELISA reader machine at 450 nm.
Measurement of EPO levels
Measurement of mouse EPO was done according to manufacturer’s instructions of the Quantikine ELISA kit for mouse/rat EPO Immunoassay (R and D Systems, Japan, Catalogue number MEP00). Briefly 50 μL of standards, control and samples were pipette into the wells of a monoclonal antibody specific for mouse/rat EPO pre-coated micro- plate, which already has 50 μL of the assay diluents added. This was incubated at RT for 2 h on a shaker. The wells were washed five times and 100 μL of the conjugate added, then incubated at RT for 2 h on the shaker. Again washing was done five times with 100 μL substrate solution added to each well and incubated for 30 min on the bench top in the dark. After 100 μL stop solution was added to each and OD read at 450 nm.
Measurement of inflammatory cytokines
Cytokines measurement was done using Procarta Mouse Cytokine Assay Kit plex according to manufacturer’s instructions (Luminex, Affymetrix). Briefly, filter plate was wetted with reading buffer and incubated at room temperature for 5 min, then filtered. Antibody beads (50 μL) were added to each well, filtered and washed once with 150 μL of washing buffer. Twenty-five microlitres of serum standard buffer was added to all the sample wells, and later equal volume (25 μL) of serum was added to each well, incubated at room temperature for 60 min. Later, washing was done three times, after which 25 μL premixed detection antibody was added, incubated for 30 min on the shaker at room temperature. After, washing and filtration was done three times. During each wash 150 μL of washing buffer was used. Streptavidin-PE (50 μL) was later added and incubated for 30 min, later washed and filtered three times. After the third wash the plate was prepared for analysis. Reading buffer (120 μL) was added to each instrument.
Measurement of transferrin
Serum transferrin was measured according to manufacturer’s instruction (ELISA kit from Alpha diagnostic International, USA, Catologue number 6390). Briefly, 100 uL of calibrators, control and samples were pipette into pre-designated wells already coated with anti-transferin antibodies, all in duplicates. This was incubated at room temperature (RT) for thirty minutes. The plate was covered during incubation. The contents of the wells were aspirated following incubation. Thereafter, each well was completely filled with diluting wash solution and aspirated. This was repeated three times, for a total of four washes. Thereafter, 100 uL of appropriately diluted enzyme-antibody conjugate was added to each well and incubated at room temperature for 30 min in the dark. The plate was covered and kept level during incubation. Washing was done and plates blotted four times as done previously. Thereafter, 100 μL of 3,3′,5,5′ tetramethylbenzidine (TMB) was added to each well and incubated for 10 min in the dark; after which 100 uL of stop solution was added to each well. The absorbance of each well was read at 450 nm.
Data analysis was done using the GraphPad Prism Version 5.00 for Windows, GraphPad Software, San Diego California, USA,. Data are expressed as the mean with standard deviation (SD) unless otherwise stated. Data were log transformed to ensure normal distribution before one-way analysis of variance (ANOVA, with Tukey’s post-test, two tailed), were performed. Pearson correlation analysis was performed on the transformed data of variables to compare the relationship between them. Values were considered significant when p < 0.05.
High levels of anti-EPO antibody in the semi-immune mice strains
Association of anti-EPO antibody with Hb loss
EPO level and its association with anti-EPO antibody
Cytokine levels and their relationship with anti-EPO antibody in the semi-immune mice strains
Cytokine levels in the semi-immune mice strains and uninfected controls
Mouse strains (number)
Uninfected control (4)
Transferrin levels in the semi-immune mice strains
To the knowledge of the authors this is the first report evaluating the levels of endogenous anti-EPO antibodies during malarial infection. The study describes a correlation between anti-EPO antibody with Hb loss. The data presented here show that anti-EPO antibody is produced during malaria infection. It is also observed in this study that host genetic factors are playing a role in the extent of anti-EPO antibody production during anaemic condition.
The positive correlation of anti-EPO antibody with %Hb loss (in Balb/c) and EPO levels in this study has been observed in another study of auto-immune condition. This study, however, do not have enough data to suggest a neutralizing effect anti-EPO antibody has on EPO during Hb loss, to keep a certain minimum amount of RBC in the pool until parasite is cleared. Further studies to evaluate that will be very informative. It is interesting to note that Balb/c which has relatively low parasitaemia, high survival rate, has a significant positive correlation of anti-EPO antibody with %Hb loss and EPO levels. The low EPO level observed in this study, indicative of low iron level; and a relationship with protection has been observed in a recent field data in humans. The explanation is that during low iron level an unfavourable internal environment is created which prevents the parasites from full proliferation. This agrees with nutritional immunity from a study on bacterial infections where protection for individuals with iron deficiency on disease severity was observed.
In this study, no significant correlation between anti-EPO antibody and the cytokine levels in all the mice strains was observed. However, it is tempting to indicate that the significantly high levels of IL-6, IL-17 and INF-γ observed in Balb/c, (Table 1), may signify synergistic effect between them and anti-EPO antibody resulting in low parasitaemia hence high survival, due to low iron level. It is not clear why similar trend of inflammatory cytokine was not observed in CBA and B6 even though similar parasitaemia was observed in them and Balb/c. Low-density parasitaemia and its treatment have been found to induce a mild increase in IL-6 and serum hepcidin concentrations. Thus the high level of IL-6 may impair bioavailability of iron resulting in low iron level leading to low parasitaemia. High levels of these two cytokines (IL-6 and INF-γ) in Balb/c suggest suppression of erythropoiesis but the mechanism(s), however, remain to be clarified. This findings support other studies where IL-6 and INF-γ were postulated to suppress erythropoiesis. Even though TNF and IL-10 are thought to contribute to the degree of anaemia in children with falciparum malaria, no significant difference was observed among the mice strains in this study, and even when compared with uninfected control. IL-17 promotes inflammation by activating cells to produce more pro-inflammatory cytokines and also thought to be associated with autoimmunity suggesting that these phenomena may be associated more with Balb/c.
The hall mark of malaria in acute cases is anaemia. This type of anaemia occurs within a very a short period and sudden. However, this study mirrors chronic infection as is the case of individuals in malaria endemic areas where persistent low Hb is observed for a relatively long period of time. Many chronic infections such as malaria are characterized by a generalized state of chronic inflammation. Furthermore, low Hb level is associated with chronic infection thus low iron level. Another way of estimating iron level in the serum is via transferrin level. Although transferrin is involved in iron trafficking[30, 31], it is also an indicator of inflammatory response. Thus, transferrin being an acute phase reactant gets elevated in inflammatory response due to malaria infection. This study concurs with this observation where in all the mice strains; transferrin level was significantly higher in the infected and recovered semi-immune mice than the uninfected level (Figure 8). Considering the extent to which these inflammatory cytokines (IL-6 and INF-γ) could be interacting with anti-EPO antibody to lower iron level, resulting in relatively low parasitaemia as discussed above; it was surprising to observe significantly low level of transferrin in Balb/c. This is because a patient with an increased serum transferrin level often suffers from iron deficiency anaemia. On the other hand a patient with decreased plasma transferrin can suffer from iron overload diseases and protein malnutrition. This shows that transferrin imbalance can have serious health effects for those with low or high serum transferrin levels. Balb/c having the least level of transferrin also suggests that they (Balb/c) had the most inflammatory process, which is backed by relatively high levels of IL-6 and INF-γ in Balb/c than the other mice strains (Table 1). Additionally, clinical significance of low transferrin level may be indicative of liver damage as a result of liver iron overdose. Also elevated levels of transferrin in the other mice strains are indicative of enhanced erythropoiesis and relatively lower inflammatory response as compared to Balb/c.
In conclusion, the data presented here show that Plasmodium infection influences anti-EPO production in all mice strains; and correlates more with Hb loss in one mice strain suggesting host factors is involved. Further studies to evaluate the kinetics of the anti-EPO antibody and its neutralization of EPO activity will help deduce and understand further the development of anaemia in malaria.
GKH is a recipient of Ph.D. scholarship from the Japanese Government Ministry of Education, Science, Sports, and Culture. This work was supported in part by a “Grand-in-Aid for Young Scientists” (17301870, 2008–2009 for NTH) from Ministry of Education, Culture, Sports, Science and Technology (MEXT) of Japan, and was supported in part by a “Grant-in-Aid for Scientific Research” from Nagasaki University to NTH (2007–2009). This study was also supported in part by Global COE Program for KH (2008–2012).
- Evans KJ, Hansen DS, van Rooijen N, Buckingham LA, Schofield L: Severe malarial anemia of low parasite burden in rodent models results from accelerated clearance of uninfected erythrocytes. Blood. 2006, 107: 1192-1199.PubMed CentralView ArticlePubMedGoogle Scholar
- Helegbe GK, Huy NT, Yanagi T, Shuaibu MN, Yamazaki A, Kikuchi M, Yasunami M, Hirayama K: Rate of red blood cell destruction varies in different strains of mice infected with Plasmodium berghei- ANKA after chronic exposure. Malar J. 2009, 8: 91-10.1186/1475-2875-8-91.PubMed CentralView ArticlePubMedGoogle Scholar
- Weatherall DJ, Abdalla S: The anaemia of Plasmodium falciparum malaria. Br Med Bull. 1982, 38: 147-151.PubMedGoogle Scholar
- Menendez C, Fleming AF, Alonso PL: Malaria-related anaemia. Parasitol Today. 2000, 16: 469-476. 10.1016/S0169-4758(00)01774-9.View ArticlePubMedGoogle Scholar
- Kurtzhals JA, Rodrigues O, Addae M, Commey JO, Nkrumah FK, Hviid L: Reversible suppression of bone marrow response to erythropoietin in Plasmodium falciparum malaria. Br J Haematol. 1997, 97: 169-174. 10.1046/j.1365-2141.1997.82654.x.View ArticlePubMedGoogle Scholar
- Yap GS, Stevenson MM: Plasmodium chabaudi AS: erythropoietic responses during infection in resistant and susceptible mice. Exp Parasitol. 1992, 75: 340-352. 10.1016/0014-4894(92)90219-Z.View ArticlePubMedGoogle Scholar
- Chang KH, Stevenson MM: Comparison of murine Epo ELISA and Epo bioassays in detecting serum Epo levels during anemia associated with malaria infection. J Immunol Meth. 2002, 262: 129-136. 10.1016/S0022-1759(02)00012-1.View ArticleGoogle Scholar
- Casadevall N, Dupuy E, Molho-Sabatier P, Tobelem G, Varet B, Mayeux P: Autoantibodies against erythropoietin in a patient with pure red-cell aplasia. NEJM. 1996, 334: 630-633. 10.1056/NEJM199603073341004.View ArticlePubMedGoogle Scholar
- Tzioufas AG, Kokori SI, Petrovas CI, Moutsopoulos HM: Autoantibodies to human recombinant erythropoietin in patients with systemic lupus erythematosus: correlation with anemia. Arthritis Rheum. 1997, 40: 2212-2216. 10.1002/art.1780401216.View ArticlePubMedGoogle Scholar
- Tsiakalos A, Kordossis T, Ziakas PD, Kontos AN, Kyriaki D, Sipsas NV: Circulating antibodies to endogenous erythropoietin and risk for HIV-1-related anemia. J Infect. 2010, 60: 238-243. 10.1016/j.jinf.2009.12.013.View ArticlePubMedGoogle Scholar
- Chang KH, Tam M, Stevenson MM: Modulation of the course and outcome of blood-stage malaria by erythropoietin-induced reticulocytosis. The J Infect Dis. 2004, 189: 735-743. 10.1086/381458.View ArticlePubMedGoogle Scholar
- Wiese L, Hempel C, Penkowa M, Kirkby N, Kurtzhals JA: Recombinant human erythropoietin increases survival and reduces neuronal apoptosis in a murine model of cerebral malaria. Malar J. 2008, 7: 3-10.1186/1475-2875-7-3.PubMed CentralView ArticlePubMedGoogle Scholar
- Moore RD, Keruly JC, Chaisson RE: Anemia and survival in HIV infection. J Acquir Immune Defic Syndr Hum Retrovirol. 1998, 19: 29-33. 10.1097/00042560-199809010-00004.View ArticlePubMedGoogle Scholar
- Spandou E, Tsouchnikas I, Karkavelas G, Dounousi E, Simeonidou C, Guiba-Tziampiri O, Tsakiris D: Erythropoietin attenuates renal injury in experimental acute renal failure ischaemic/reperfusion model. Nephrol Dial Transplant. 2006, 21: 330-336. 10.1093/ndt/gfi177.View ArticlePubMedGoogle Scholar
- Brines ML, Ghezzi P, Keenan S, Agnello D, de Lanerolle NC, Cerami C, Itri LM, Cerami A: Erythropoietin crosses the blood–brain barrier to protect against experimental brain injury. Proc Natl Acad Sci USA. 2000, 97: 10526-10531. 10.1073/pnas.97.19.10526.PubMed CentralView ArticlePubMedGoogle Scholar
- Erslev AJ: Erythropoietin titers in health and disease. Semin Hematol. 1991, 28: 2-7. discussion 7–8PubMedGoogle Scholar
- Harrison PR: Haemopoiesis: molecular control of Haemopoiesis. 1991, Chichester: John Wiley & Sons, Ltd ednGoogle Scholar
- Casadevall N, Nataf J, Viron B, Kolta A, Kiladjian JJ, Martin-Dupont P, Michaud P, Papo T, Ugo V, Teyssandier I, Varet B, Mayeux P: Pure red-cell aplasia and antierythropoietin antibodies in patients treated with recombinant erythropoietin. NEJM. 2002, 346: 469-475. 10.1056/NEJMoa011931.View ArticlePubMedGoogle Scholar
- Tsubata S, Ebe K, Kawamura T, Ishimoto Y, Tomiyama-Miyaji C, Watanabe H, Sekikawa H, Aoyagi Y, Abo T: Protection against malaria by anti-erythropoietin antibody due to suppression of erythropoiesis in the liver and at other sites. Immunol Cell Biol. 2005, 83: 638-642. 10.1111/j.1440-1711.2005.01385.x.View ArticlePubMedGoogle Scholar
- Collicutt NB, Grindem CB, Neel JA: Comparison of manual polychromatophilic cell and automated reticulocyte quantification in evaluating regenerative response in anemic dogs. Vet Clin Pathol. 2012, 41: 256-260. 10.1111/j.1939-165X.2012.00432.x.View ArticlePubMedGoogle Scholar
- GraphPad Prism version 5.00 for Windows. [http://www.graphpad.com/]
- Akanmori BD, Kurtzhals JA, Goka BQ, Adabayeri V, Ofori MF, Nkrumah FK, Behr C, Hviid L: Distinct patterns of cytokine regulation in discrete clinical forms of Plasmodium falciparum malaria. Eur Cytokine Netw. 2000, 11: 113-118.PubMedGoogle Scholar
- Othoro C, Lal AA, Nahlen B, Koech D, Orago AS, Udhayakumar V: A low interleukin-10 tumor necrosis factor-alpha ratio is associated with malaria anemia in children residing in a holoendemic malaria region in western Kenya. J Infect Dis. 1999, 179: 279-282. 10.1086/314548.View ArticlePubMedGoogle Scholar
- Gwamaka M, Kurtis JD, Sorensen BE, Holte S, Morrison R, Mutabingwa TK, Fried M, Duffy PE: Iron deficiency protects against severe Plasmodium falciparum malaria and death in young children. Clin Infect Dis. 2012, 54: 1137-1144. 10.1093/cid/cis010.PubMed CentralView ArticlePubMedGoogle Scholar
- Awah NW, Kaneko A: Iron deficiency and severe Plasmodium falciparum malaria. Clin Infect Dis. 2012, 54: 1145-1147. 10.1093/cid/cis020.PubMed CentralView ArticlePubMedGoogle Scholar
- de Mast Q, van Dongen-Lases EC, Swinkels DW, Nieman AE, Roestenberg M, Druilhe P, Arens TA, Luty AJ, Hermsen CC, Sauerwein RW, van der Ven AJ: Mild increases in serum hepcidin and interleukin-6 concentrations impair iron incorporation in haemoglobin during an experimental human malaria infection. Br J Haematol. 2009, 145: 657-664. 10.1111/j.1365-2141.2009.07664.x.View ArticlePubMedGoogle Scholar
- Zarychanski R, Houston DS: Anemia of chronic disease: a harmful disorder or an adaptive, beneficial response?. CMAJ. 2008, 179: 333-337.PubMed CentralView ArticlePubMedGoogle Scholar
- Chang SH, Dong C: A novel heterodimeric cytokine consisting of IL-17 and IL-17F regulates inflammatory responses. Cell Res. 2007, 17: 435-440.PubMedGoogle Scholar
- Zhao L, Tang Y, You Z, Wang Q, Liang S, Han X, Qiu D, Wei J, Liu Y, Shen L, Chen X, Peng Y, Li Z, Ma X: Interleukin-17 contributes to the pathogenesis of autoimmune hepatitis through inducing hepatic interleukin-6 expression. PLoS One. 2011, 6: e18909-10.1371/journal.pone.0018909.PubMed CentralView ArticlePubMedGoogle Scholar
- Moos T, Rosengren Nielsen T, Skjorringe T, Morgan EH: Iron trafficking inside the brain. J Neurochem. 2007, 103: 1730-1740. 10.1111/j.1471-4159.2007.04976.x.View ArticlePubMedGoogle Scholar
- Mayle KM, Le AM, Kamei DT: The intracellular trafficking pathway of transferrin. Biochim Biophys Acta. 1820, 2012: 264-281.Google Scholar
- Haddad G, Belosevic M: Transferrin-derived synthetic peptide induces highly conserved pro-inflammatory responses of macrophages. Mol Immunol. 2009, 46: 576-586. 10.1016/j.molimm.2008.07.030.View ArticlePubMedGoogle Scholar
- Macedo MF, de Sousa M: Transferrin and the transferrin receptor: of magic bullets and other concerns. Inflamm Allergy Drug Targets. 2008, 7: 41-52. 10.2174/187152808784165162.View ArticlePubMedGoogle Scholar
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