Familial Haploidentical (FHI) Allogeneic Stem Cell Transplantation Utilizing CD34 Enrichment and T Cell Addback in Children, Adolescents & Adults with High-Risk Sickle Cell Disease. Rapid Engraftment, Low Incidence of Agvhd, and Sustained Donor Chimerism

Mitchell S. Cairo; Julie-An M. Talano; Theodore B. Moore; Rona Weinberg; Carolyn A. Keever-Taylor; Brenda Grossman; Lee Ann Baxter-Lowe; Susan K. Parsons; Suzanne Braniecki; Erin Morris; Phyllis Brand; Sandra Fabricatore; Janet Ayello; Mildred Semidei-Pomales; Carmella van de Ven; Cori Abikoff; Shalini Shenoy

doi:10.1016/j.bbmt.2015.11.876

Familial Haploidentical (FHI) Allogeneic Stem Cell Transplantation Utilizing CD34 Enrichment and T Cell Addback in Children, Adolescents & Adults with High-Risk Sickle Cell Disease. Rapid Engraftment, Low Incidence of Agvhd, and Sustained Donor Chimerism

Biology of Blood and Marrow Transplantation ◽

10.1016/j.bbmt.2015.11.876 ◽

2016 ◽

Vol 22 (3) ◽

pp. S367-S368 ◽

Cited By ~ 2

Author(s):

Mitchell S. Cairo ◽

Julie-An M. Talano ◽

Theodore B. Moore ◽

Rona Weinberg ◽

Carolyn A. Keever-Taylor ◽

...

Keyword(s):

Stem Cell ◽

T Cell ◽

High Risk ◽

Sickle Cell Disease ◽

Stem Cell Transplantation ◽

Cell Transplantation ◽

Sickle Cell ◽

Allogeneic Stem Cell Transplantation ◽

Cell Disease ◽

Low Incidence

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Robust Donor Chimerism and Engraftment Following Familial Haploidentical (FHI) (CD34 Enriched and T-Cell Addback) Allogeneic Stem Cell Transplantation in Patients with High Risk Sickle Cell Disease (SCD)

Biology of Blood and Marrow Transplantation ◽

10.1016/j.bbmt.2015.11.396 ◽

2016 ◽

Vol 22 (3) ◽

pp. S95-S96 ◽

Cited By ~ 2

Author(s):

Darcy Hamill ◽

Lee Ann Baxter-Lowe ◽

Shalini Shenoy ◽

Theodore B. Moore ◽

Erin Morris ◽

...

Keyword(s):

Stem Cell ◽

T Cell ◽

High Risk ◽

Sickle Cell Disease ◽

Stem Cell Transplantation ◽

Cell Transplantation ◽

Sickle Cell ◽

Allogeneic Stem Cell Transplantation ◽

Cell Disease ◽

Donor Chimerism

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Immune Reconstitution in Children and Adolescents with High Risk Sickle Cell Disease (SCD) after Familial Haploidentical (FHI) Allogeneic Stem Cell Transplantation (AlloSCT) Utilizing CD34 Enrichment and PB MNC Addback (Ind 14359)

Biology of Blood and Marrow Transplantation ◽

10.1016/j.bbmt.2017.12.438 ◽

2018 ◽

Vol 24 (3) ◽

pp. S428-S429

Author(s):

Yaya Chu ◽

James Verbsky ◽

Julie-An M. Talano ◽

Erin Morris ◽

Janet Ayello ◽

...

Keyword(s):

Stem Cell ◽

High Risk ◽

Sickle Cell Disease ◽

Stem Cell Transplantation ◽

Children And Adolescents ◽

Cell Transplantation ◽

Sickle Cell ◽

Allogeneic Stem Cell Transplantation ◽

Immune Reconstitution ◽

Cell Disease

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Familial Haploidentical (FHI) T-Cell Depleted (TCD) with T-Cell Addback Stem Cell Transplantation for Patients with High-Risk Sickle Cell Disease (SCD) (IND 14359)

Biology of Blood and Marrow Transplantation ◽

10.1016/j.bbmt.2016.12.480 ◽

2017 ◽

Vol 23 (3) ◽

pp. S246-S247

Author(s):

Julie-An M. Talano ◽

Cori Abikoff ◽

Carolyn A. Keever-Taylor ◽

Mark C. Walters ◽

Shalini Shenoy ◽

...

Keyword(s):

Stem Cell ◽

T Cell ◽

High Risk ◽

Sickle Cell Disease ◽

Stem Cell Transplantation ◽

Cell Transplantation ◽

Sickle Cell ◽

Cell Disease

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Familial Haploidentical (FHI) T-Cell Depleted (TCD) with T-Cell Addback Stem Cell Transplantation for Patients with High-Risk Sickle Cell Disease (SCD) (IND 14359)

Biology of Blood and Marrow Transplantation ◽

10.1016/j.bbmt.2013.12.208 ◽

2014 ◽

Vol 20 (2) ◽

pp. S135-S136 ◽

Cited By ~ 2

Author(s):

Julie-An Talano ◽

Carolyn Keever-Taylor ◽

Mark Walters ◽

Shalini Shenoy ◽

Theodore B. Moore ◽

...

Keyword(s):

Stem Cell ◽

T Cell ◽

High Risk ◽

Sickle Cell Disease ◽

Stem Cell Transplantation ◽

Cell Transplantation ◽

Sickle Cell ◽

Cell Disease

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Treatment of High-Risk Sickle Cell Disease (SCD) with Familial Haploidentical (FHI) T-Cell Depleted (TCD) Stem Cell Transplantation with T-Cell Addback (IND 14359)

Biology of Blood and Marrow Transplantation ◽

10.1016/j.bbmt.2014.11.110 ◽

2015 ◽

Vol 21 (2) ◽

pp. S90-S91 ◽

Cited By ~ 1

Author(s):

Cori Abikoff ◽

Julie-An Talano ◽

Carolyn Keever-Taylor ◽

Mark Walters ◽

Shalini Shenoy ◽

...

Keyword(s):

Stem Cell ◽

T Cell ◽

High Risk ◽

Sickle Cell Disease ◽

Stem Cell Transplantation ◽

Cell Transplantation ◽

Sickle Cell ◽

Cell Disease

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T-cell deplete versus T-cell replete haploidentical hematopoietic stem cell transplantation for sickle cell disease: where are we?

Expert Review of Hematology ◽

10.1080/17474086.2019.1642103 ◽

2019 ◽

Vol 12 (9) ◽

pp. 733-752 ◽

Cited By ~ 1

Author(s):

Dilan A. Patel ◽

Adeseye M. Akinsete ◽

James A. Connelly ◽

Adetola A. Kassim

Keyword(s):

Stem Cell ◽

T Cell ◽

Sickle Cell Disease ◽

Hematopoietic Stem Cell Transplantation ◽

Stem Cell Transplantation ◽

Cell Transplantation ◽

Hematopoietic Stem Cell ◽

Sickle Cell ◽

Cell Disease ◽

Hematopoietic Stem

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Long Term Organ Stability and Outcome in Children and Adolescents With Sickle Cell Disease (SCD) Following Reduced Toxicity Conditioning (RTC) Allogeneic Stem Cell Transplantation (SCT)

Biology of Blood and Marrow Transplantation ◽

10.1016/j.bbmt.2010.12.087 ◽

2011 ◽

Vol 17 (2) ◽

pp. S180-S181 ◽

Cited By ~ 3

Author(s):

M. Bhatia ◽

M.B. Geyer ◽

C. Baker ◽

W.A. Zuckerman ◽

D. Duffy ◽

...

Keyword(s):

Stem Cell ◽

Sickle Cell Disease ◽

Stem Cell Transplantation ◽

Children And Adolescents ◽

Cell Transplantation ◽

Sickle Cell ◽

Allogeneic Stem Cell Transplantation ◽

Cell Disease ◽

Reduced Toxicity

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A Pilot Study of Reduced Intensity Conditioning (RI) with Busulfan (Bu), Fludarabine (Flu), and Alemtuzumab Followed by Allogeneic Stem Cell Transplantation (AlloSCT) to Induce Sustained Mixed Donor Chimerism in Patients With Symptomatic Sickle Cell Disease (SCD)

Biology of Blood and Marrow Transplantation ◽

10.1016/j.bbmt.2008.12.072 ◽

2009 ◽

Vol 15 (2) ◽

pp. 23-24 ◽

Cited By ~ 1

Author(s):

M. Bhatia ◽

E. Morris ◽

V. Moore ◽

B. Tallamy ◽

D. George ◽

...

Keyword(s):

Stem Cell ◽

Pilot Study ◽

Sickle Cell Disease ◽

Stem Cell Transplantation ◽

Cell Transplantation ◽

Sickle Cell ◽

Allogeneic Stem Cell Transplantation ◽

Cell Disease ◽

Reduced Intensity Conditioning ◽

Reduced Intensity

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Determining the Safety and Efficacy of Prophylactic Defibrotide Administration in Children, Adolescents, and Young Adults with Sickle Cell Disease Following Myeloimmunoablative Conditioning (MAC) and Haploidentical Stem Cell Transplantation Utilizing CD34+ Selection and T-Cell (CD3) Addback (IND127812)

Biology of Blood and Marrow Transplantation ◽

10.1016/j.bbmt.2019.12.525 ◽

2020 ◽

Vol 26 (3) ◽

pp. S212-S213

Author(s):

Jordan Milner ◽

Justine Hung ◽

Janet Ayello ◽

Qiuhu Shi ◽

Julie-An M. Talano ◽

...

Keyword(s):

Young Adults ◽

Stem Cell ◽

T Cell ◽

Sickle Cell Disease ◽

Stem Cell Transplantation ◽

Cell Transplantation ◽

Sickle Cell ◽

Cell Disease ◽

Safety And Efficacy ◽

Cd34 Selection

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221: Preliminary Results of Non-Ablative Conditioning (NAC) with Busulfan (Bu), Fludarabine (Flu) and Alemtuzumab followed by Allogeneic Stem Cell Transplantation (AlloSCT) to Induce Mixed Donor Chimerism in Patients with Sickle Cell Disease (SCD)

Biology of Blood and Marrow Transplantation ◽

10.1016/j.bbmt.2007.12.230 ◽

2008 ◽

Vol 14 (2) ◽

pp. 82-83 ◽

Cited By ~ 1

Author(s):

M. Bhatia ◽

L. Baldinger ◽

G. Billote ◽

E. Morris ◽

M.B. Bradley ◽

...

Keyword(s):

Stem Cell ◽

Sickle Cell Disease ◽

Stem Cell Transplantation ◽

Cell Transplantation ◽

Sickle Cell ◽

Allogeneic Stem Cell Transplantation ◽

Cell Disease ◽

Preliminary Results ◽

Donor Chimerism

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