Literature DB >> 16555613

Stem cells: the next therapeutic frontier.

H David Humes1.   

Abstract

Cell therapy is one of the most exciting fields in translational medicine. It stands at the intersection of a variety of rapidly developing scientific disciplines: stem cell biology, immunology, tissue engineering, molecular biology, biomaterials, transplantation biology, regenerative medicine, and clinical research. Cell-based therapy may develop into a new therapeutic platform to treat a vast array of clinical disorders. Blood transfusions and bone marrow transplantation are prime examples of the successful application of cell-based therapeutics; but recent advances in cellular and molecular biology have expanded the potential applications of this approach. Although recombinant genetic engineering to produce a variety of therapeutics such as human erythropoietin and insulin has proven successful, these treatments are unable to completely correct or reverse disease states, because most common disease processes are not due to the deficiency of a single protein but develop due to alterations in the complex interactions of a variety of cell components. In these complex situations, cell-based therapy may be a more successful strategy by providing a dynamic, interactive, and individualized therapeutic approach that responds to the pathophysiological condition of the patient. In this regard, cells may provide innovative methods for drug delivery of biologics, immunotherapy, and tissue regenerative or replacement engineering (1,2). The translation of this discipline to medical practice has tremendous potential, but in many applications technological issues need to be overcome. Since many cell-based indications are already being evaluated in the clinic, the field appears to be on the threshold of a number of successes. This review will focus on our group's use of human stem/progenitor cells in the treatment of acute and chronic renal failure as extensions to the current successful renal substitution processes of hemodialysis and hemofiltration.

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Mesh:

Year:  2005        PMID: 16555613      PMCID: PMC1473140     

Source DB:  PubMed          Journal:  Trans Am Clin Climatol Assoc        ISSN: 0065-7778


  66 in total

Review 1.  Gene-based approaches to the treatment of hemophilia.

Authors:  Katherine High
Journal:  Ann N Y Acad Sci       Date:  2002-06       Impact factor: 5.691

2.  A serious adverse event after successful gene therapy for X-linked severe combined immunodeficiency.

Authors:  Salima Hacein-Bey-Abina; Christof von Kalle; Manfred Schmidt; Françoise Le Deist; Nicolas Wulffraat; Elisabeth McIntyre; Isabelle Radford; Jean-Luc Villeval; Christopher C Fraser; Marina Cavazzana-Calvo; Alain Fischer
Journal:  N Engl J Med       Date:  2003-01-16       Impact factor: 91.245

3.  Cell encapsulation: promise and progress.

Authors:  Gorka Orive; Rosa María Hernández; Alicia R Gascón; Riccardo Calafiore; Thomas M S Chang; Paul De Vos; Gonzalo Hortelano; David Hunkeler; Igor Lacík; A M James Shapiro; José Luis Pedraz
Journal:  Nat Med       Date:  2003-01       Impact factor: 53.440

4.  Transplanted bone marrow regenerates liver by cell fusion.

Authors:  George Vassilopoulos; Pei-Rong Wang; David W Russell
Journal:  Nature       Date:  2003-03-30       Impact factor: 49.962

5.  Cell fusion is the principal source of bone-marrow-derived hepatocytes.

Authors:  Xin Wang; Holger Willenbring; Yassmine Akkari; Yumi Torimaru; Mark Foster; Muhsen Al-Dhalimy; Eric Lagasse; Milton Finegold; Susan Olson; Markus Grompe
Journal:  Nature       Date:  2003-03-30       Impact factor: 49.962

6.  Bioartificial kidney ameliorates gram-negative bacteria-induced septic shock in uremic animals.

Authors:  William H Fissell; Liandi Lou; Simin Abrishami; Deborah A Buffington; H David Humes
Journal:  J Am Soc Nephrol       Date:  2003-02       Impact factor: 10.121

7.  Initial clinical results of the bioartificial kidney containing human cells in ICU patients with acute renal failure.

Authors:  H David Humes; William F Weitzel; Robert H Bartlett; Fresca C Swaniker; Emil P Paganini; Jack R Luderer; Joseph Sobota
Journal:  Kidney Int       Date:  2004-10       Impact factor: 10.612

8.  Enhanced MHC class II expression in renal proximal tubules precedes loss of renal function in MRL/lpr mice with lupus nephritis.

Authors:  R P Wuthrich; M A Yui; G Mazoujian; N Nabavi; L H Glimcher; V E Kelley
Journal:  Am J Pathol       Date:  1989-01       Impact factor: 4.307

9.  Cell therapy with a tissue-engineered kidney reduces the multiple-organ consequences of septic shock.

Authors:  H David Humes; Deborah A Buffington; Liandi Lou; Simin Abrishami; Min Wang; Jun Xia; William H Fissell
Journal:  Crit Care Med       Date:  2003-10       Impact factor: 7.598

10.  Expression of HLA antigens on renal tubular cells in culture. II. Effect of increased HLA antigen expression on tubular cell stimulation of lymphocyte activation and on their vulnerability to cell-mediated lysis.

Authors:  G A Bishop; J A Waugh; B M Hall
Journal:  Transplantation       Date:  1988-08       Impact factor: 4.939

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  4 in total

Review 1.  Scaffolding in tissue engineering: general approaches and tissue-specific considerations.

Authors:  B P Chan; K W Leong
Journal:  Eur Spine J       Date:  2008-11-13       Impact factor: 3.134

2.  Fast and mild strategy, using superhydrophobic surfaces, to produce collagen/platelet lysate gel beads for skin regeneration.

Authors:  Ana Catarina Lima; João F Mano; Angel Concheiro; Carmen Alvarez-Lorenzo
Journal:  Stem Cell Rev Rep       Date:  2015-02       Impact factor: 5.739

3.  Bioartificial Kidneys.

Authors:  Peter R Corridon; In Kap Ko; James J Yoo; Anthony Atala
Journal:  Curr Stem Cell Rep       Date:  2017-04-12

4.  IKVAV regulates ERK1/2 and Akt signalling pathways in BMMSC population growth and proliferation.

Authors:  B Li; T Qiu; P Zhang; X Wang; Y Yin; S Li
Journal:  Cell Prolif       Date:  2014-04       Impact factor: 6.831

  4 in total

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