Production of Polyclonal Antibody against Recombinant Growth Hormone and Designing an ELISA Kit and Comparing Some of its Diagnostics Indices with a Commercial Kit

Document Type : Original Article (s)

Authors

1 MSc Student, Department of Immunology, School of Medicine AND Student Research Committee, Isfahan University of Medical Sciences, Isfahan, Iran

2 Associate Professor, Department of Immunology, School of Medicine AND Cellular and Molecular Immunology Research Center, Isfahan University of Medical Sciences, Isfahan AND Department of Biology, School of Sciences, University of Isfahan, Isfahan, Iran

3 PhD Student, Department of Epidemiology, School of Health and Nutrition, Shiraz University of Medical Sciences, Shiraz, Iran

4 Assistant Professor, Department of Anatomical Sciences and Molecular Biology, School of Medicine AND Pediatrics Inherited Diseases Research Center, Isfahan University of Medical Sciences, Isfahan, Iran

5 Assistant Professor, Department of Immunology, School of Medicine, Isfahan University of Medical Sciences, Isfahan, Iran

Abstract

Background: Human growth hormone (hGH) is a secretory protein of the blood which is used extensively in biotechnology and medical sciences. Recombinant human growth hormone production is still one of the priorities of the Iranian Ministry of Health. One of the most sensitive and accurate techniques for the measurement of this hormone is the ELISA method. Scientists need to produce antibody against hGH to measure the serum level of hGH in patients. Commercial ELISA kits are commonly imported from other countries to Iran. Therefore, the current study aimed to produce a polyclonal antibody against hGH in order to make a domestic ELISA kit to measure this hormone.Methods: Rabbit polyclonal antibody against hGH was produced following 10 weeks of immunization by the antigen injection. The antibody characteristics were evaluated by immunoblotting. The purified antibody was used to design the ELISA kit. The designed sandwich ELISA method was standardized concerning the amount of antibody coating and antibody conjugate. Ultimately, the sensitivity and specificity of the designed kit was compared with the foreign kits.Findings: The polyclonal antibody against hGH was produced in rabbits and purified successfully. This antibody can be used in the western blot and ELISA methods. The diagnostic value of the designed kit was 98%, compared with the foreign kits.Conclusion: This kit has a diagnostic value in the assessment of hGH; therefore, it can be a good alternative to the commercial kits. Therefore, this antibody and ELISA kit can be produced more cost-effectively and can be a step towards self-sufficiency. 

Keywords


  1. Shalet SM, Rahim A, Toogood AA. Growth hormone therapy for adult growth hormone deficiency. Trends Endocrinol Metab 1996; 7(8): 287-90.
  2. Hattori N, Saito T, Yagyu T, Jiang BH, Kitagawa K, Inagaki C. GH, GH receptor, GH secretagogue receptor, and ghrelin expression in human T cells, B cells, and neutrophils. J Clin Endocrinol Metab 2001; 86(9): 4284-91.
  3. Corpas E, Harman SM, Blackman MR. Human growth hormone and human aging. Endocr Rev 1993; 14(1): 20-39.
  4. Cassorla F, Cianfarani S, Haverkamp F, Labarta JI, Loche S, Luo X, et al. Growth hormone and treatment outcomes: expert review of current clinical practice. Pediatr Endocrinol Rev 2011; 9(2): 554-65.
  5. Voller A, Bidwell DE, Bartlett A. Enzyme immunoassays in diagnostic medicine. Theory and practice. Bull World Health Organ 1976; 53(1): 55-65.
  6. Popii V, Baumann G. Laboratory measurement of growth hormone. Clin Chim Acta 2004; 350(1-2): 1-16.
  7. Andersen M, Petersen PH, Blaabjerg O, Hangaard J, Hagen C. Evaluation of growth hormone assays using ratio plots. Clin Chem 1998; 44(5): 1032-8.
  8. Kitano K, Fukuda Y, Nagahira K, Nasu T, Noguchi C, Izumi R, et al. Production of polyclonal antibody specific for human natriuretic peptide receptor B. J Immunol Methods 1996; 194(2): 147-53.
  9. Melchior F. Generation and purification of rabbit or goat polyclonal antibodies. Melchior's lab protocols 2002 [Online]. [cited 2013]; Available from: http://www.rubicon-net.org/data/file/716_EN_generationandpurificationofrabbitorgoatpolyclonalantibodies.pdf.
  10. Diestre C, Martinez-Lorenzo MJ, Bosque A, Naval J, Larrad L, Anel A. Generation of rabbit antibodies against death ligands by cDNA immunization. J Immunol Methods 2006; 317(1-2): 12-20.
  11. Cooper HM, Paterson Y. Production of polyclonal antisera. Curr Protoc Immunol 2001; Chapter 2: Unit.
  12. Zhang S, Xiang J, Cheng A, Wang M, Li X, Li L, et al. Production, purification and characterization of polyclonal antibody against the truncated gK of the duck enteritis virus. Virol J 2010; 7: 241.
  13. Wadhwa M, Thorpe R, Bird CR, Gearing AJ. Production of polyclonal and monoclonal antibodies to human granulocyte colony-stimulating factor (GCSF) and development of immunoassays. J Immunol Methods 1990; 128(2): 211-7.
  14. Ostler EL, Resmini M, Brocklehurst K, Gallacher G. Polyclonal catalytic antibodies. J Immunol Methods 2002; 269(1-2): 111-24.
  15. Kurpisz M, Gupta SK, Fulgham DL, Alexander NJ. Production of large amounts of mouse polyclonal antisera. J Immunol Methods 1988; 115(2): 195-8.
  16. Jean J, Turcotte C, Simard RE, Fliss I. Production and characterization of polyclonal antibodies against cholecalciferol (vitamin D3). J Immunol Methods 1999; 223(2): 155-63.
  17. Stott DI. Immunoblotting and dot blotting. J Immunol Methods 1989; 119(2): 153-87.
  18. Prasad S, Thraves P, Kanai Y, Smulson M, Dritschilo A. A dot-blot method for screening polyclonal and monoclonal antisera to poly(ADP-ribose). J Immunol Methods 1989; 116(1): 79-85.
  19. Nakazawa M, Mukumoto M, Miyatake K. Production and purification of polyclonal antibodies. Methods Mol Biol 2010; 657: 63-74.
  20. Andrew SM, Titus JA. Purification of immunoglobulin G.In: Current protocols in cell biology. New York, NY: John Wiley & Sons, Inc.; 2001.
  21. Hong TH, Chen ST, Tang TK, Wang SC, Chang TH. The production of polyclonal and monoclonal antibodies in mice using novel immunization methods. J Immunol Methods 1989; 120(2): 151-7.
  22. Samavati N, Mirjalili A, Boutorabi M. An indirect enzyme-linked immunosorbent assay to detect antibodies against brucellosis in cattle or humans. J Isfahan Med Sch 2012; 30(205): 1403-14. [In Persian].
  23. Paulie S, Perlmann H, Perlmann P. Enzyme-linked Immunosorbent Assay. eLS. New York, NY: John Wiley & Sons, Ltd; 2001.
  24. Rezaei M, Zarkesh-Esfahani SM. Production of recombinant human growth hormone by eukaryotic CHO cell and measurement of its biological activity by gene reporter assay. Razi J Med Sci 2013; 19(104): 1-9. [In Persian].
  25. Crowther J. ELISA Theory and practice: Humanupress Totowa New Jersey; 1995.
  26. Yaseri MM, Pakpour Haji A, Rahmani S, Rangin H, Akaberi A, Yekani Nejad MS. Self-Learning concepts of diagnostic tests by graphical approach: sensitivity, specificity, positive predictive value and negative predictive value. J North Khorasan Univ Med Sci 2012; 4(2): 275-82. [In Persian].
  27. Hashimoto Y, Ikeda I, Ikeda M, Takahashi Y, Hosaka M, Uchida H, et al. Construction of a specific and sensitive sandwich enzyme immunoassay for 20 kDa human growth hormone. J Immunol Methods 1998; 221(1-2): 77-85.
  28. Barazesh A, Madjidi J, Fallah E, Jamali R, Ghazanchaei A, Abdolalizadeh J. Prodution of polyclonal antibody against giardia Lamblia in rabbit. J Ilam Univ Med Sci 2006; 14(4): 26-31. [In Persian].
  29. Alizadeh H, Alizadeh H, Alizadeh H, Alizadeh H, Golchinfar F, Emami T. Preparation and purification of polyclonal antibodies against mycobacterium avium paratuberculosis antigens in rabbit. J Fasa Univ Med Sci 2012; 2(3): 168-73. [In Persian].
  30. Kaboutari J, Arab HA, Foroumadi A, Nikbakht GR, Taheri M. Polyclonal antibody production against bovine serum albuminconjugated artemisinin in rabbit. Iranian Journal of Veterinary Medicine 2008; 2(1): 87-94. [In Persian].
  31. Zare N, Zarkesh Esfahani SH, Shaygannejad V, Gharagozloo M. Designing of an ELISA method for the measurement of serum antibodies against interferon-beta and the study of the frequency of these antibodies in patients with multiple sclerosis treated with CinnoVex. J Isfahan Med Sch 2012; 30(207): 1481-91. [In Persian].