Fig. 1 Illustration showing reconstruction of segmental bone loss using vascularized bone allotransplantation in an animal model. During allotransplantation, the nutrient blood supply is repaired and allogeneic vascularized tissue is implanted within the medullary canal. Only short-term immunosuppression is required, because angiogenesis creates a new autogenous blood supply. Used with permission of Mayo Foundation for Medical Education and Research. All rights reserved.


Published 3/1/2015
Amy Kile

Research: A Recipe for Better Care

Early funding from OREF leads to successful research career, improved treatments

Research is vital for finding solutions. That’s the mantra of Allen T. Bishop, MD, professor of orthopaedics at the Mayo Clinic Department of Orthopedics, Rochester, Minn.

“The payoff comes as we learn something new that affects clinical practice,” Dr. Bishop said. “Orthopaedic surgeons need research to find solutions to the diverse problems they face when treating patients.”

A series of small grants and assistance from established researchers William P. Cooney III, MD, and Michael B. Wood, MD, encouraged Dr. Bishop to seek independent funding while working in Mayo’s Microsurgical Research Laboratory. He turned to the Orthopaedic Research and Education Foundation (OREF).

“OREF helped me in two very important ways,” he said. “The most significant was the Career Development Award [now called Career Development Grant]. The other was the Grant Writing Workshop [now cosponsored by the Orthopaedic Research Society and AAOS and called the New Investigator Workshop].”

The Career Development Award provided 2 years’ funding for Dr. Bishop’s fledgling laboratory effort, “Cellular Survival, Repopulation, and Neoangiogenesis in Ischemic Bone.” That research resulted in several published manuscripts, including a large-animal study that demonstrated the superiority of vascularized bone grafts in treating carpal nonunions that have an avascular proximal segment. The study also showed that blood flow from the interposed vascularized bone restored circulation within adjacent necrotic bone segments. This validated the use of similar grafts in scaphoid nonunions and became widely accepted in clinical practice.

Additional research showed that an arteriovenous pedicle implanted in necrotic iliac crest bone in rabbits rapidly sprouted a new intraosseous vascular bed and that the extent and speed of this process could be further stimulated by growth factor delivery.

Constructive criticism
These studies provided a framework for subsequent National Institutes of Health (NIH) funding. During the “eye-opening” Grant Writing Workshop, Dr. Bishop learned to write, revise, and refine a research grant proposal, which was reviewed by faculty and other workshop participants.

“They tore my initial grant to shreds,” Dr. Bishop recalled. Cato T. Laurencin, MD, PhD, Dr. Bishop’s assigned mentor, reviewed the grant’s strengths and weaknesses in detail and advised him on improvements. Dr. Bishop took these suggestions to heart, ultimately writing 25 more drafts.

With additional guidance from his Mayo Clinic colleagues Mark E. Bolander, MD, and Kenton R. Kaufman, PhD, Dr. Bishop finally submitted the proposal to the NIH. All of the refining paid off. He received an impact/priority score of 9, resulting in R01 grant funding on his first submission—a very rare occurrence.

“It was exhausting, but I have to credit OREF for the opportunity, and the faculty at the grant writing workshop for their constructive criticism. It wasn’t pleasant at the time, but it was necessary,” he said.

The OREF funding, additional grants from the Musculoskeletal Transplant Foundation, many small grants, and two successful renewals of his R01 grant have provided continual funding for Dr. Bishop’s work.

Bench-to-bedside collaborations
Problems encountered in clinical practice have been the impetus for all of Dr. Bishop’s experimental studies. “Orthopaedic surgeons are in a unique position to perform applied research directed to an identified clinical problem,” said Dr. Bishop. However, success depends upon building a team of research fellows and basic science collaborators.

“I find making a research plan to be similar to cooking,” he said. “I know what I want to make, but need to find the best recipe or technique to address a specific hypothesis and/or aim. Collaborations with biomechanical engineers, molecular biologists, and immunologists are necessary. Often, an initial plan does not work and requires modification, much as a chef modifies an unsuccessful recipe.”

Dissatisfaction with results in treating carpal osteonecrosis and scaphoid nonunions provided the basis for Dr. Bishop to investigate angiogenesis in bone. “The scaphoid has always been a difficult bone. It’s surrounded by joint fluid, covered in articular cartilage over most of its surface, and has a problem with its blood supply. Yet it is the most commonly fractured wrist bone,” he explained.

With his OREF funding, Dr. Bishop studied better methods for treating scaphoid fractures using vascularized bone grafting. His findings led to changes in clinical practice, followed by subsequent reevaluation of clinical outcomes. The transfer of research findings to clinical practice has led to improvements in treating scaphoid nonunions and Kienbock’s disease, an interruption in the blood supply to the lunate bone in the wrist.

One treatment—transferring a pedicle of blood vessels from the end of the radius into the scaphoid to vascularize the transplanted bone—had had some success. Yet when Dr. Bishop applied this method in practice, he found that it was only 70 percent effective, especially in cases in which the scaphoid length was not restored to its original dimensions or when the proximal pole was small and fragmented.

He hypothesized that the amount and quality of distal radius bone was insufficient to adequately restore scaphoid length and correct the resultant carpal instability. He tried an alternative—a distal femoral medial condylar flap, using an anatomic study to identify the best harvest site. Results, which have been analyzed and published, were better than the radius pedicle grafts.

Although some issues still need resolving, the use of vascularized bone grafting is now widely accepted if prior surgery was unsuccessful or if the fracture is not healing properly because of osteonecrosis of the proximal scaphoid pole.

Continuing to advance
The NIH grant enabled Dr. Bishop to take the research he’d begun with OREF funding to the next level.

He and his research team have investigated ways to maintain viability of allogeneic bone and joint transplants without need for lifelong immunosuppression, which is expensive and, with prolonged use, may result in metabolic problems, osteonecrosis, opportunistic infections, and neoplasm.

“In our alternative method, we replace or switch the circulation from the original allogeneic bone vasculature with a newly developed, or neoangiogenic, autologous circulation provided by implantation of vascularized tissue from the recipient at the time of microsurgical transplantation,” he explained.

Dr. Bishop accomplishes this by reconstructing a segment of missing femur or tibia with a size- and shape-matched fresh allogeneic bone, transplanted with microsurgical repair of the bone nutrient blood supply in a fashion identical to a standard vascularized fibular autograft (Fig. 1). In addition, adjacent autogenous vascularized tissue—an arteriovenous bundle or fascial flap, depending on the specific animal model—is placed within the bone.

So far, Dr. Bishop has shown that angiogenesis from the implanted tissue will quickly grow into the transplanted bone, maintaining measurable bone blood flow, osteocyte viability, and active bone remodeling. Thus, only short-term immunosuppression—generally 2 weeks—is needed. Thereafter, even though the allogeneic nutrient vessels are rejected, the new blood supply maintains bone circulation.

Through sex-mismatched transplants, Dr. Bishop has shown that the bone remodeling and healing that occur following bone allotransplantation are the result of circulation-derived cells from the recipient, not from the surviving cells of the transplanted organ.

Dr. Bishop currently is investigating graft and systemic immunologic responses to bone allotransplantation in a Yucatan minipig model. He will compare the results of bone allotransplantation to those from conventional cryopreserved allograft reconstruction. If successful, these results will provide a basis for ethical application in clinic and show how research begun with funding from OREF can improve clinical practice.

“I think my research team has contributed to our understanding of vascularized bone grafts, the benefits of angiogenesis to treat osteonecrosis and revitalize structural allografts, and the future potential of living bone allotransplantation in orthopaedic practice,” Dr. Bishop said. His close collaboration with Alexander Y. Shin, MD, has resulted in a new direction of investigation, focused on improving the results of peripheral nerve repair, paralleling their clinical practice of treating brachial plexus injury.

“OREF can and does support research that changes clinical practice and improves outcomes for patients,” Dr. Bishop said. “But without financial support of orthopaedic clinicians, those of us who do the research probably wouldn’t get started. OREF funding gives us the chance to develop a substantial, long-lasting research career.”

Amy Kile is the communications manager for OREF. She can be reached at