Engineered tendon graft for rotator cuff repair
The present disclosure relates to tissue engineering, and more particularly to a method for treating or repairing rotator cuff or other tendon tears or damage using scaffold-free 3-dimensional engineered tendon constructs.
1. A rotator cuff repair construct that is a scaffold-free, tissue-engineered tendon construct derived from growing cells in culture that establishes native enthesis in vivo after implantation, comprising:
i) a bone-fixation end, wherein the bone-fixation end comprises a single column of tendon tissue for fixation to bone in a tendon repair surgery and at the opposite end the column branches to form a tendon-fixation end of the tendon construct; and
ii) a tendon-fixation end having two or more tendon prongs each having a free end for fixation to a tendon in a tendon repair surgery and at the opposite end the prong ends fuse to form one end of the bone-fixation end of the construct,
wherein the bone-fixation end regenerates a native enthesis at the interface of the bone and the rotator cuff repair construct, wherein the native enthesis includes a fibrocartilage region having graded zones.
2. The rotator cuff repair construct of claim 1 , wherein the bone-fixation end has a diameter of approximately 3-6 mm and wherein the diameter of each of the tendon-fixation end prongs is approximately 2-3 mm.
3. The rotator cuff repair construct of claim 1 , wherein the bone-fixation end is from about 2-7 cm in length.
4. The rotator cuff repair construct of claim 1 , wherein the length of each of the tendon-fixation end prongs is approximately 1-5 cm.
5. The rotator cuff repair construct of claim 1 , wherein the tendon-fixation end prongs start at about one-half (½) to two-thirds (⅔) of the length of the entire construct.
6. The rotator cuff repair construct of claim 1 , wherein the tendon-fixation end has 2, 3, 4 or 5 prongs.